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Acetaminophen and Codeine Phosphate - 68084-372-01 - (Acetaminophen and Codeine Phosphate)

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Drug Information of Acetaminophen and Codeine Phosphate

Product NDC: 68084-372
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: 68084-372
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089805
Marketing Category: ANDA
Start Marketing Date: 20100113

Package Information of Acetaminophen and Codeine Phosphate

Package NDC: 68084-372-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-372-01) > 10 TABLET in 1 BLISTER PACK (68084-372-11)

NDC Information of Acetaminophen and Codeine Phosphate

NDC Code 68084-372-01
Proprietary Name Acetaminophen and Codeine Phosphate
Package Description 10 BLISTER PACK in 1 CARTON (68084-372-01) > 10 TABLET in 1 BLISTER PACK (68084-372-11)
Product NDC 68084-372
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen and Codeine Phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100113
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 30
Strength Unit mg/1; mg/1
Pharmaceutical Classes Full Opioid Agonists [MoA],Opioid Agonist [EPC]

Complete Information of Acetaminophen and Codeine Phosphate


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