Home > National Drug Code (NDC) > Acetaminophen and Codeine Phosphate

Acetaminophen and Codeine Phosphate - 51079-161-21 - (Acetaminophen and Codeine Phosphate)

Alphabetical Index


Drug Information of Acetaminophen and Codeine Phosphate

Product NDC: 51079-161
Proprietary Name: Acetaminophen and Codeine Phosphate
Non Proprietary Name: Acetaminophen and Codeine Phosphate
Active Ingredient(s): 300; 30    mg/1; mg/1 & nbsp;   Acetaminophen and Codeine Phosphate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen and Codeine Phosphate

Product NDC: 51079-161
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088628
Marketing Category: ANDA
Start Marketing Date: 20120216

Package Information of Acetaminophen and Codeine Phosphate

Package NDC: 51079-161-21
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-161-21) > 1 TABLET in 1 BLISTER PACK (51079-161-01)

NDC Information of Acetaminophen and Codeine Phosphate

NDC Code 51079-161-21
Proprietary Name Acetaminophen and Codeine Phosphate
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-161-21) > 1 TABLET in 1 BLISTER PACK (51079-161-01)
Product NDC 51079-161
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen and Codeine Phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120216
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 30
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Acetaminophen and Codeine Phosphate


General Information