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Hydrocodone Bitartate and Acetaminophen - 68788-9754-9 - (HYDROCODONE BITARTRATE, ACETAMINOPHEN)

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Drug Information of Hydrocodone Bitartate and Acetaminophen

Product NDC: 68788-9754
Proprietary Name: Hydrocodone Bitartate and Acetaminophen
Non Proprietary Name: HYDROCODONE BITARTRATE, ACETAMINOPHEN
Active Ingredient(s): 325; 2.5    mg/1; mg/1 & nbsp;   HYDROCODONE BITARTRATE, ACETAMINOPHEN
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydrocodone Bitartate and Acetaminophen

Product NDC: 68788-9754
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040846
Marketing Category: ANDA
Start Marketing Date: 20120814

Package Information of Hydrocodone Bitartate and Acetaminophen

Package NDC: 68788-9754-9
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (68788-9754-9)

NDC Information of Hydrocodone Bitartate and Acetaminophen

NDC Code 68788-9754-9
Proprietary Name Hydrocodone Bitartate and Acetaminophen
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (68788-9754-9)
Product NDC 68788-9754
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDROCODONE BITARTRATE, ACETAMINOPHEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120814
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 325; 2.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Opioid Agonist [EPC],Opioid Agonists [MoA]

Complete Information of Hydrocodone Bitartate and Acetaminophen


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