Vicodin - 12634-129-91 - (HYDROCODONE BITARTRATE)

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Drug Information of Vicodin

Product NDC: 12634-129
Proprietary Name: Vicodin
Non Proprietary Name: HYDROCODONE BITARTRATE
Active Ingredient(s): 750; 7.5    mg/1; mg/1 & nbsp;   HYDROCODONE BITARTRATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Vicodin

Product NDC: 12634-129
Labeler Name: Apotheca, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089736
Marketing Category: ANDA
Start Marketing Date: 20091214

Package Information of Vicodin

Package NDC: 12634-129-91
Package Description: 1 TABLET in 1 BLISTER PACK (12634-129-91)

NDC Information of Vicodin

NDC Code 12634-129-91
Proprietary Name Vicodin
Package Description 1 TABLET in 1 BLISTER PACK (12634-129-91)
Product NDC 12634-129
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCODONE BITARTRATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091214
Marketing Category Name ANDA
Labeler Name Apotheca, Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 750; 7.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Vicodin


General Information