Pain
📧 Sign up to get email alerts when something new happens for Pain.
Sign up freeTop drugs studied for this disease
-
FDA approval · 2009-10-08FDA Approved: BUPRENORPHINE — Original Application (Hikma Pharmaceuticals USA Inc.)
FDA approved Hikma Pharmaceuticals USA Inc.'s original application for buprenorphine, a generic opioid medication, under the ANDA pathway. T…
-
FDA approval · 2009-07-16FDA Approved: CODEINE SULFATE — Original Application (Hikma Pharmaceuticals USA Inc.)
FDA approves Codeine Sulfate under an Original Application for Hikma Pharmaceuticals USA Inc. for use as an analgesic to relieve pain.
-
FDA approval · 2009-05-19FDA Approved: ADVIL PM — Supplemental Application (Haleon US Holdings LLC)
FDA approved a supplemental application for Advil PM (diphenhydramine HCl and ibuprofen) submitted by Haleon US Holdings LLC.
-
FDA approval · 2009-05-19FDA Approved: JUNIOR STRENGTH ADVIL — Supplemental Application (Haleon US Holdings LLC)
FDA approved a supplemental application for Junior Strength Advil (ibuprofen) from Haleon US Holdings LLC.
-
FDA approval · 2009-05-01FDA Approved: BUTORPHANOL TARTRATE — Original Application (Hikma Pharmaceuticals USA Inc.)
The FDA approves a generic version of butorphanol tartrate under an original application for Hikma Pharmaceuticals USA Inc.
- Want full summaries, importance scores, and drug timelines? Upgrade to Plus or Pro.
-
FDA approval · 2009-04-29FDA Approved: INFANTS MOTRIN — Supplemental Application (Kenvue Brands LLC)
The FDA approved a supplemental application for Infants Motrin (ibuprofen) from Kenvue Brands LLC. This action pertains to the infant formul…
-
FDA approval · 2009-03-24FDA Approved: IBUPROFEN — Original Application (DOLGENCORP INC)
The FDA approved DolGenCorp Inc's original application for ibuprofen, establishing a generic ibuprofen product (capsules, including liquid-f…
-
FDA approval · 2009-01-14FDA Approved: ETODOLAC — Supplemental Application (Taro Pharmaceuticals U.S.A., Inc.)
FDA approved a supplemental application for etodolac filed by Taro Pharmaceuticals U.S.A., Inc., authorizing changes to labeling and/or manu…
-
FDA approval · 2008-10-06FDA Approved: KETOROLAC TROMETHAMINE — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved Sun Pharmaceutical Industries' ketorolac tromethamine as a generic injectable NSAID for short-term management of acute pain.
-
FDA approval · 2008-08-22FDA Approved: GOOD SENSE CHILDRENS IBUPROFEN — Supplemental Application (L. Perrigo Company)
FDA approved a supplemental application for Good Sense Children’s Ibuprofen (ibuprofen) from L. Perrigo Company.
-
FDA approval · 2008-07-25FDA Approved: NAPROXEN — Supplemental Application (Zameer Pharmaceuticals LLC)
The FDA has approved a supplemental application for naproxen filed by Zameer Pharmaceuticals LLC.
-
FDA approval · 2008-06-27FDA Approved: FEVERALL CHILDRENS — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for FEVERALL CHILDRENS (acetaminophen) from Sun Pharmaceutical Industries, expanding the product…
-
FDA approval · 2008-06-20FDA Approved: JUNIOR STRENGTH ADVIL — Supplemental Application (Haleon US Holdings LLC)
FDA approves a supplemental application for JUNIOR STRENGTH ADVIL (ibuprofen) from Haleon US Holdings LLC.
-
FDA approval · 2008-05-09FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
The FDA approved a supplemental application for a generic hydrocodone bitartrate and acetaminophen product from Sun Pharmaceutical Industrie…
-
FDA approval · 2008-03-20FDA Approved: HYDROCODONE BITARTRATE AND IBUPROFEN — Supplemental Application (Amneal Pharmaceuticals of New York LLC)
FDA approved a supplemental application for Hydrocodone Bitartrate and Ibuprofen by Amneal Pharmaceuticals of New York LLC, approving this h…
-
FDA approval · 2008-03-17FDA Approved: MORPHINE SULFATE — Original Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved Morphine Sulfate under Hikma Pharmaceuticals USA Inc.'s Original Application (NDA 022195), authorizing the marketing of thi…
-
FDA approval · 2008-01-26FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (SpecGx LLC)
FDA approved a supplemental application for methadone hydrochloride from SpecGx LLC, enabling another generic version of the product.
-
FDA approval · 2008-01-26FDA Approved: OXYCODONE AND ACETAMINOPHEN — Supplemental Application (SpecGx LLC)
FDA approved a supplemental application for a generic oxycodone hydrochloride and acetaminophen product manufactured by SpecGx LLC.
-
FDA approval · 2008-01-14FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for Methadone Hydrochloride submitted by Hikma Pharmaceuticals USA Inc.
-
FDA approval · 2008-01-02FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for methadone hydrochloride from Hikma Pharmaceuticals USA Inc., authorizing changes included in…
-
FDA approval · 2008-01-02FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for methadone hydrochloride (generic) submitted by Hikma Pharmaceuticals USA Inc.
-
FDA approval · 2007-12-14FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (VistaPharm, LLC)
FDA approved a supplemental application for Methadone Hydrochloride from VistaPharm, LLC, resulting in a supplemental approval for this gene…
-
FDA approval · 2007-11-28FDA Approved: IBUPROFEN CHILDRENS — Supplemental Application (Rite Aid Corporation)
FDA approves a supplemental application for IBUPROFEN CHILDRENS from Rite Aid Corporation, indicating an approved amendment to an already ma…
-
FDA approval · 2007-11-09FDA Approved: BUTALBITAL, ASPIRIN, CAFFEINE AND CODEINE PHOSPHATE — Supplemental Application (Amneal Pharmaceuticals of New York, LLC)
FDA approved a supplemental application for the generic formulation of Butalbital, Aspirin, Caffeine and Codeine Phosphate by Amneal Pharmac…
-
FDA approval · 2007-11-07FDA Approved: NAPROXEN — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for Naproxen (generic Naproxen) from Hikma Pharmaceuticals USA Inc., resulting in approval of a gene…