FDA Application
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NDC Search Results on Active Ingredient: acetaminophen
Click on Active Ingredient to view the label.
Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
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OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 70710-1330-5 | Zydus Pharmaceuticals (USA) Inc. | ANDA210079 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 70710-1328-1 | Zydus Pharmaceuticals (USA) Inc. | ANDA210079 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; BUTALBITAL; ACETAMINOPHEN | 70710-1378-1 | Zydus Pharmaceuticals (USA) Inc. | ANDA211543 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70710-1329-1 | Zydus Pharmaceuticals (USA) Inc. | ANDA210079 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 70710-1328-5 | Zydus Pharmaceuticals (USA) Inc. | ANDA210079 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70710-1329-5 | Zydus Pharmaceuticals (USA) Inc. | ANDA210079 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 70710-1330-1 | Zydus Pharmaceuticals (USA) Inc. | ANDA210079 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70710-1327-1 | Zydus Pharmaceuticals (USA) Inc. | ANDA210079 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 68382-334-10 | Zydus Pharmaceuticals USA Inc. | ANDA090460 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 68382-334-01 | Zydus Pharmaceuticals USA Inc. | ANDA090460 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 68382-334-05 | Zydus Pharmaceuticals USA Inc. | ANDA090460 | HUMAN PRESCRIPTION DRUG | ANDA |
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