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Acetaminophen and Codeine Phosphate - 0093-0350-05 - (Acetaminophen and Codeine Phosphate)

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Drug Information of Acetaminophen and Codeine Phosphate

Product NDC: 0093-0350
Proprietary Name: Acetaminophen and Codeine Phosphate
Non Proprietary Name: Acetaminophen and Codeine Phosphate
Active Ingredient(s): 300; 60    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: 0093-0350
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088629
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Acetaminophen and Codeine Phosphate

Package NDC: 0093-0350-05
Package Description: 500 TABLET in 1 BOTTLE (0093-0350-05)

NDC Information of Acetaminophen and Codeine Phosphate

NDC Code 0093-0350-05
Proprietary Name Acetaminophen and Codeine Phosphate
Package Description 500 TABLET in 1 BOTTLE (0093-0350-05)
Product NDC 0093-0350
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acetaminophen and Codeine Phosphate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name ACETAMINOPHEN; CODEINE PHOSPHATE
Strength Number 300; 60
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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