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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ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1011-0 | H.J. Harkins Company, Inc. | ANDA040846 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1011-1 | H.J. Harkins Company, Inc. | ANDA040846 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1011-2 | H.J. Harkins Company, Inc. | ANDA040846 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1011-3 | H.J. Harkins Company, Inc. | ANDA040846 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1011-4 | H.J. Harkins Company, Inc. | ANDA040846 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1011-5 | H.J. Harkins Company, Inc. | ANDA040846 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1011-6 | H.J. Harkins Company, Inc. | ANDA040846 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1011-7 | H.J. Harkins Company, Inc. | ANDA040846 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1011-8 | H.J. Harkins Company, Inc. | ANDA040846 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1011-9 | H.J. Harkins Company, Inc. | ANDA040846 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 76519-1079-3 | H.J. Harkins Company, Inc. | ANDA090415 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1081-1 | H.J. Harkins Company, Inc. | ANDA090415 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1081-3 | H.J. Harkins Company, Inc. | ANDA090415 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 76519-1081-4 | H.J. Harkins Company, Inc. | ANDA090415 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE | 76864-208-01 | Procaps S.A. de C.V. | part341 | HUMAN OTC DRUG | OTC monograph final |
PHENYLEPHRINE HYDROCHLORIDE, (+/-)-; GUAIFENESIN; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 76864-220-04 | Procaps S.A. de C.V. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 77800-100-01 | HealthRight Products, LLC | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 78527-014-01 | RAPHA HEALTH NETWORK INTERNATIONAL INC | part343 | HUMAN OTC DRUG | OTC monograph not final |
ASPIRIN; ACETAMINOPHEN; CAFFEINE | 78612-100-20 | Marga Labs, LLC | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
ACETAMINOPHEN; ASPIRIN; CAFFEINE | 78612-110-20 | Marga Labs, LLC | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
ACETAMINOPHEN | 79395-282-04 | Chalkboard Health Inc | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 79481-0026-2 | MEIJER, INC | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
DOXYLAMINE SUCCINATE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 79481-0027-2 | Meijer, Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DOXYLAMINE SUCCINATE; DEXTROMETHORPHAN HYDROBROMIDE | 79481-0030-4 | Meijer, Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 79481-0045-1 | Meijer Distribution, Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 79481-0183-2 | MEIJER DISTRIBUTION INC | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 79481-0183-4 | MEIJER DISTRIBUTION INC | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 79481-0183-5 | MEIJER DISTRIBUTION INC | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 79481-0184-1 | MEIJER, INC. | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 79481-0184-8 | MEIJER, INC. | ANDA211544 | HUMAN OTC DRUG | ANDA |
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