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Hydrocodone Bitartrate and Acetaminophen - 0904-3440-61 - (Hydrocodone Bitartrate and Acetaminophen)

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Drug Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 0904-3440
Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Non Proprietary Name: Hydrocodone Bitartrate and Acetaminophen
Active Ingredient(s): 500; 5    mg/1; mg/1 & nbsp;   Hydrocodone Bitartrate and Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocodone Bitartrate and Acetaminophen

Product NDC: 0904-3440
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089883
Marketing Category: ANDA
Start Marketing Date: 19881201

Package Information of Hydrocodone Bitartrate and Acetaminophen

Package NDC: 0904-3440-61
Package Description: 100 TABLET in 1 BLISTER PACK (0904-3440-61)

NDC Information of Hydrocodone Bitartrate and Acetaminophen

NDC Code 0904-3440-61
Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Package Description 100 TABLET in 1 BLISTER PACK (0904-3440-61)
Product NDC 0904-3440
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate and Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19881201
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 500; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Hydrocodone Bitartrate and Acetaminophen


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