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Hydrocodone Bitartrate And Acetaminophen - 68788-9137-2 - (Hydrocodone Bitartrate And Acetaminophen)

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Drug Information of Hydrocodone Bitartrate And Acetaminophen

Product NDC: 68788-9137
Proprietary Name: Hydrocodone Bitartrate And Acetaminophen
Non Proprietary Name: Hydrocodone Bitartrate And Acetaminophen
Active Ingredient(s): 325; 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: 68788-9137
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040655
Marketing Category: ANDA
Start Marketing Date: 20090909

Package Information of Hydrocodone Bitartrate And Acetaminophen

Package NDC: 68788-9137-2
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (68788-9137-2)

NDC Information of Hydrocodone Bitartrate And Acetaminophen

NDC Code 68788-9137-2
Proprietary Name Hydrocodone Bitartrate And Acetaminophen
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (68788-9137-2)
Product NDC 68788-9137
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocodone Bitartrate And Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090909
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
Strength Number 325; 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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