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Acetaminophen; codeine phosphateis the generic ingredient in seventeen branded drugs marketed by Teva, Robins Ah, Solvay, Ortho Mcneil Pharm, Aci Healthcare Ltd, Actavis Mid Atlantic, Anda Repository, Dava Pharms Inc, Hi Tech Pharma, Lannett Co Inc, Pharm Assoc, Wockhardt Bio Ag, Valeant Pharms Llc, Able, Am Therap, Amneal Pharms Ny, Aurolife Pharma Llc, Duramed Pharms Barr, Elite Labs Inc, Everylife, Eywa, Fosun Pharma, Halsey, Kv Pharm, Lederle, Mikart, Mutual Pharm, Puracap Pharm, Purepac Pharm, Rhodes Pharms, Roxane, Sandoz, Specgx Llc, Sun Pharm Inds Ltd, Superpharm, Usl Pharma, Valeant Pharm Intl, Vintage, Vintage Pharms, Vitarine, Warner Chilcott, Watson Labs, Watson Labs Florida, Whiteworth Town Plsn, Carnrick, Glaxosmithkline, Vangard, and Janssen Pharms, and is included in one hundred and ten NDAs. Additional information is available in the individual branded drug profile pages.
There are sixty-six drug master file entries for acetaminophen; codeine phosphate. Forty-six suppliers are listed for this compound.
Recent Clinical Trials for acetaminophen; codeine phosphate
Identify potential brand extensions & 505(b)(2) entrants
|Roxane Laboratories||Phase 1|
Pharmacology for acetaminophen; codeine phosphate
|Drug Class||Opioid Agonist |
|Mechanism of Action||Full Opioid Agonists |
Synonyms for acetaminophen; codeine phosphate
|Applicant||Tradename||Generic Name||Dosage||NDA||Approval Date||TE||Type||RLD||RS||Patent No.||Patent Expiration||Product||Substance||Delist Req.||Exclusivity Expiration|
|Kv Pharm||ACETAMINOPHEN AND CODEINE PHOSPHATE||acetaminophen; codeine phosphate||TABLET;ORAL||085288-001||Approved Prior to Jan 1, 1982||DISCN||No||No||Start Trial||Start Trial||Start Trial|
|Vintage Pharms||ACETAMINOPHEN AND CODEINE PHOSPHATE||acetaminophen; codeine phosphate||TABLET;ORAL||089828-001||Sep 30, 1988||AA||RX||No||No||Start Trial||Start Trial||Start Trial|
|Teva||ACETAMINOPHEN AND CODEINE PHOSPHATE||acetaminophen; codeine phosphate||TABLET;ORAL||088627-001||Mar 6, 1985||AA||RX||No||No||Start Trial||Start Trial||Start Trial|
|>Applicant||>Tradename||>Generic Name||>Dosage||>NDA||>Approval Date||>TE||>Type||>RLD||>RS||>Patent No.||>Patent Expiration||>Product||>Substance||>Delist Req.||>Exclusivity Expiration|
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