Pain
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Sign up freeTop drugs studied for this disease
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FDA approval · 2011-06-22FDA Approved: ACETAMINOPHEN AND CODEINE PHOSPHATE — Supplemental Application (Strides Pharma Science Limited)
FDA approved a supplemental application for Acetaminophen and Codeine Phosphate by Strides Pharma Science Limited, approving changes to labe…
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FDA approval · 2011-06-22FDA Approved: ACETAMINOPHEN AND CODEINE PHOSPHATE — Supplemental Application (SpecGx LLC)
FDA approved a supplemental application for Acetaminophen and Codeine Phosphate from SpecGx LLC.
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FDA approval · 2011-04-26FDA Approved: INFANTS ADVIL — Supplemental Application (Haleon US Holdings LLC)
FDA approved a supplemental application for Infants Advil (ibuprofen) from Haleon US Holdings LLC. The approval updates the product's labeli…
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FDA approval · 2011-01-21FDA Approved: GOOD SENSE CHILDRENS IBUPROFEN — Supplemental Application (L. Perrigo Company)
The FDA approved a supplemental application for Good Sense Children's Ibuprofen from L. Perrigo Company.
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FDA approval · 2010-11-22FDA Approved: TRAMADOL HYDROCHLORIDE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved Teva Pharmaceuticals USA, Inc.'s supplemental application for tramadol hydrochloride, supporting its generic analgesic product.
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FDA approval · 2010-11-15FDA Approved: OXYCONTIN — Supplemental Application (Purdue Pharma LP)
The FDA approved a supplemental application for OxyContin (oxycodone hydrochloride) submitted by Purdue Pharma LP.
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FDA approval · 2010-11-01FDA Approved: TAPENTADOL — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental NDA for tapentadol hydrochloride by Hikma Pharmaceuticals USA Inc., allowing a generic version of tapentadol to …
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FDA approval · 2010-09-24FDA Approved: BUPRENORPHINE HYDROCHLORIDE — Original Application (PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma)
FDA approved a generic buprenorphine hydrochloride product under an Original Application (ANDA 090622) from PAI Holdings/PAI Pharma. This ma…
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FDA approval · 2010-09-01FDA Approved: ADVIL PM- DIPHENHYDRAMINE CITRATE AND IBUPROFEN TABLET, COATED — Supplemental Application (Lil Drug Store Products, Inc)
The FDA approved a supplemental application for Advil PM, a coated tablet containing diphenhydramine citrate and ibuprofen. The sponsor is L…
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FDA approval · 2010-08-12FDA Approved: NAPROXEN SODIUM — Supplemental Application (Bionpharma Inc.)
The FDA approved a supplemental application for Naproxen Sodium submitted by Bionpharma Inc.
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FDA approval · 2010-08-06FDA Approved: ACETAMINOPHEN FOR CHILDREN — Supplemental Application (Padagis Israel Pharmaceuticals Ltd)
FDA approved a supplemental application for Acetaminophen for Children, submitted by Padagis Israel Pharmaceuticals Ltd, indicating an appro…
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FDA approval · 2010-08-06FDA Approved: ACETAMINOPHEN PAIN RELIEVER FEVER REDUCER — Supplemental Application (Padagis Israel Pharmaceuticals Ltd)
FDA approved a supplemental application for Padagis Israel Pharmaceuticals Ltd for Acetaminophen Pain Reliever Fever Reducer, validating its…
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FDA approval · 2010-07-15FDA Approved: INFANTS MOTRIN — Supplemental Application (Kenvue Brands LLC)
The FDA approved a supplemental application for Infants Motrin (ibuprofen) filed by Kenvue Brands LLC.
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FDA approval · 2010-07-14FDA Approved: OXYCODONE HYDROCHLORIDE — Supplemental Application (SpecGx LLC)
The FDA approved a supplemental application for oxycodone hydrochloride from SpecGx LLC, indicating approval of a generic oxycodone HCl prod…
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FDA approval · 2010-07-06FDA Approved: DICLOFENAC SODIUM — Supplemental Application (Edenbridge Pharmaceuticals LLC.)
FDA approved a supplemental application for diclofenac sodium from Edenbridge Pharmaceuticals LLC under the ANDA program. This action consti…
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FDA approval · 2010-06-30FDA Approved: BUTRANS — Original Application (Purdue Pharma LP)
FDA approved Purdue Pharma's original NDA for BUTRANS, a buprenorphine transdermal patch, for the treatment of moderate to severe chronic pa…
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FDA approval · 2010-06-14FDA Approved: OXYMORPHONE HYDROCHLORIDE — Original Application (Amneal Pharmaceuticals of New York LLC)
FDA approved Oxymorphone hydrochloride from Amneal Pharmaceuticals of New York LLC as an original application, making a generic oxymorphone …
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FDA approval · 2010-05-14FDA Approved: SPRIX — Original Application (Zyla Life Sciences US LLC)
FDA approved SPRIX (ketorolac tromethamine) from Zyla Life Sciences US LLC through an Original Application, authorizing a short-term analges…
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FDA approval · 2010-05-11FDA Approved: MS CONTIN — Supplemental Application (Rhodes Pharmaceuticals L.P.)
FDA approved a supplemental application for MS CONTIN (morphine sulfate) from Rhodes Pharmaceuticals L.P., under NDA 19516.
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FDA approval · 2010-05-07FDA Approved: TRAMADOL HYDROCHLORIDE EXTENDED-RELEASE — Original Application (Trigen Laboratories, LLC)
The FDA approved Tramadol hydrochloride extended-release (Trigen Laboratories) under Original Application NDA 022370 for pain management req…
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FDA approval · 2010-04-05FDA Approved: OXYCONTIN — Original Application (Purdue Pharma LP)
The FDA approved the original application for OxyContin (oxycodone hydrochloride) by Purdue Pharma LP for relief of moderate to severe pain.
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FDA approval · 2010-02-25FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Original Application (Hikma Pharmaceuticals USA Inc.)
FDA approved the original application for HYDROCODONE BITARTRATE AND ACETAMINOPHEN tablets from Hikma Pharmaceuticals USA Inc., a generic co…
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FDA approval · 2009-11-09FDA Approved: METHADOSE DISPERSIBLE — Supplemental Application (SpecGx LLC)
FDA approved a supplemental application for Methadose Dispersible (methadone hydrochloride) from SpecGx LLC, authorizing the dispersible dos…
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FDA approval · 2009-11-05FDA Approved: KETOROLAC TROMETHAMINE — Original Application (Apotex Corp.)
FDA approved Ketorolac Tromethamine from Apotex Corp. under an original ANDA, enabling a generic version of this analgesic. It is indicated …
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FDA approval · 2009-11-05FDA Approved: KETOROLAC TROMETHAMINE — Original Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved Sun Pharmaceutical's original ANDA for a generic ketorolac tromethamine product, enabling its sale for short-term analgesia…