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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BUTALBITAL; CAFFEINE; ACETAMINOPHEN | 76420-802-60 | Asclemed USA, Inc. | ANDA209587 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; BUTALBITAL; CAFFEINE | 71205-510-60 | Proficient Rx LP | ANDA209587 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; BUTALBITAL; ACETAMINOPHEN | 70518-2995-1 | REMEDYREPACK INC. | ANDA209587 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; BUTALBITAL; ACETAMINOPHEN | 70518-2995-0 | REMEDYREPACK INC. | ANDA209587 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; ACETAMINOPHEN; CAFFEINE | 50268-553-11 | AvPAK | ANDA209587 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CAFFEINE; BUTALBITAL | 50090-7042-0 | A-S Medication Solutions | ANDA209587 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; BUTALBITAL; CAFFEINE | 71205-510-90 | Proficient Rx LP | ANDA209587 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 70710-1330-5 | Zydus Pharmaceuticals (USA) Inc. | ANDA210079 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70710-1328-1 | Zydus Pharmaceuticals (USA) Inc. | ANDA210079 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 70710-1327-1 | Zydus Pharmaceuticals (USA) Inc. | ANDA210079 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70710-1329-1 | 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 | 70710-1329-5 | Zydus Pharmaceuticals (USA) Inc. | ANDA210079 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 70710-1328-5 | Zydus Pharmaceuticals (USA) Inc. | ANDA210079 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 71335-1970-5 | Bryant Ranch Prepack | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 68071-3447-3 | NuCare Pharmaceuticals,Inc. | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 71930-020-13 | Eywa Pharma Inc | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 71335-2144-1 | Bryant Ranch Prepack | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 71335-1970-1 | Bryant Ranch Prepack | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 63629-8885-3 | Bryant Ranch Prepack | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 71335-2116-1 | Bryant Ranch Prepack | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 63629-8885-5 | Bryant Ranch Prepack | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 71930-020-12 | Eywa Pharma Inc | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 60687-396-11 | American Health Packaging | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 71930-019-13 | Eywa Pharma Inc | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 72162-1990-5 | Bryant Ranch Prepack | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 71335-1970-3 | Bryant Ranch Prepack | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 71930-020-52 | Eywa Pharma Inc | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 68071-2762-6 | NuCare Pharmaceuticals,Inc. | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 71335-2144-7 | Bryant Ranch Prepack | ANDA210211 | HUMAN PRESCRIPTION DRUG | ANDA |
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