Pain
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Sign up freeTop drugs studied for this disease
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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.
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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.
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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.
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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…
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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.
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CLINICAL_TRIALS trial_result · 2007-12-27Clinical Trial Update: Reduction of Topical Anesthetic Onset Time Using Ultrasound [Phase 4]
Phase 4 clinical trial completed evaluating whether ultrasound can shorten the onset time of a topical anesthetic.
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CLINICAL_TRIALS trial_result · 2007-12-17Clinical Trial Update: Minimum Local Anesthetic Volume of Bupivacaine in Labour Epidurals [NA]
This clinical trial update reports on a completed study evaluating the minimum volume of local anesthetic (bupivacaine) used in labor epidur…
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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…
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FDA label_change · 2007-11-30FDA Approved: ACETAMINOPHEN AND CODEINE PHOSPHATE — Supplemental Application (SpecGx LLC)
FDA approved a supplemental application for Acetaminophen and Codeine Phosphate submitted by SpecGx LLC.
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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…
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CLINICAL_TRIALS research · 2007-11-16Clinical Trial Update: Descriptive Study of Pain, Anxiety and Depression
A completed descriptive clinical trial examining pain, anxiety, and depression, sponsored by the Danish Pain Research Center.
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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…
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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…
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CLINICAL_TRIALS trial_result · 2007-09-05Clinical Trial Update: Auricular Acupuncture for Acute Pain [NA]
This update notes the completed status of a clinical trial evaluating auricular acupuncture for acute pain, sponsored by the Samueli Institu…
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FDA approval · 2007-08-16FDA Approved: HYDROCODONE BITARTRATE AND ACETAMINOPHEN — Original Application (Sun Pharmaceutical Industries, Inc.)
FDA approved Sun Pharmaceutical's generic hydrocodone bitartrate and acetaminophen for relief of moderate to moderately severe acute pain. T…
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FDA approval · 2007-07-23FDA Approved: OXYCODONE AND ACETAMINOPHEN — Supplemental Application (SpecGx LLC)
FDA approved a supplemental application for the fixed-dose combination of oxycodone hydrochloride and acetaminophen from SpecGx LLC.
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FDA approval · 2007-06-19FDA Approved: KETOROLAC TROMETHAMINE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved Teva's supplemental application for ketorolac tromethamine, a generic NSAID.
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FDA approval · 2007-06-07FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for generic methadone hydrochloride from Hikma Pharmaceuticals USA Inc.
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FDA approval · 2007-06-07FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
FDA approved a supplemental application for Methadone Hydrochloride from Hikma Pharmaceuticals USA Inc., indicating approval of a generic pr…
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CLINICAL_TRIALS trial_result · 2007-05-31Clinical Trial Update: Use of Sedation and Local Anesthesia in Meatotomy: A Prospective Comparison Study [Phase 3]
A Phase 3 prospective trial compares sedation and local anesthesia approaches for meatotomy; the snippet does not provide results or status …
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FDA approval · 2007-05-11FDA Approved: MS CONTIN — Supplemental Application (Rhodes Pharmaceuticals L.P.)
FDA approved a supplemental application for MS CONTIN (morphine sulfate) submitted by Rhodes Pharmaceuticals L.P.
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FDA approval · 2007-05-09FDA Approved: METHADONE HYDROCHLORIDE — Supplemental Application (Hikma Pharmaceuticals USA Inc.)
The FDA approved a supplemental application for methadone hydrochloride, a generic product manufactured by Hikma Pharmaceuticals USA Inc., u…
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FDA approval · 2007-04-18FDA Approved: PRIALT — Supplemental Application (TerSera Therapeutics LLC)
FDA approved a supplemental application for PRIALT (ziconotide acetate) submitted by TerSera Therapeutics LLC.
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FDA approval · 2007-04-04FDA Approved: METHADOSE DISPERSIBLE — Supplemental Application (SpecGx LLC)
FDA approved a supplemental application for METHADOSE DISPERSIBLE (methadone hydrochloride) by SpecGx LLC, introducing a dispersible formula…
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FDA approval · 2007-03-28FDA Approved: NAPROXEN — Original Application (Glenmark Pharmaceuticals Inc., USA)
FDA approved Glenmark's naproxen generic under an original ANDA, enabling market access for generic naproxen products.