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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DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 70692-602-12 | Strive Pharmaceuticals Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 70692-150-31 | Strive Pharmaceuticals Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 70692-141-42 | Strive Pharmaceuticals Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
CAFFEINE; ASPIRIN; ACETAMINOPHEN | 70692-142-31 | Strive Pharmaceuticals Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 70692-150-20 | Strive Pharmaceuticals Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; DOXYLAMINE SUCCINATE; DEXTROMETHORPHAN HYDROBROMIDE | 70692-808-48 | Strive Pharmaceuticals Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE | 70692-809-74 | Strive Pharmaceuticals Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; ASPIRIN; CAFFEINE | 70692-132-20 | Strive Pharmaceuticals Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN | 70692-133-82 | Strive Pharmaceuticals Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; CAFFEINE; PYRILAMINE MALEATE | 70692-131-46 | Strive Pharmaceuticals Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 70692-150-44 | Strive Pharmaceuticals Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 70692-399-06 | Strive Pharmaceuticals Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 57664-537-88 | Sun Pharmaceutical Industries, Inc. | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 63304-562-10 | Sun Pharmaceutical Industries, Inc. | ANDA085868 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 63304-561-01 | Sun Pharmaceutical Industries, Inc. | ANDA087083 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 63304-497-03 | Sun Pharmaceutical Industries, Inc. | ANDA040826 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 63304-497-10 | Sun Pharmaceutical Industries, Inc. | ANDA040826 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 63304-562-01 | Sun Pharmaceutical Industries, Inc. | ANDA085868 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 57664-537-13 | Sun Pharmaceutical Industries, Inc. | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 63304-497-05 | Sun Pharmaceutical Industries, Inc. | ANDA040826 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 63304-562-05 | Sun Pharmaceutical Industries, Inc. | ANDA085868 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 63304-497-11 | Sun Pharmaceutical Industries, Inc. | ANDA040826 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 63304-561-05 | Sun Pharmaceutical Industries, Inc. | ANDA087083 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 57664-537-18 | Sun Pharmaceutical Industries, Inc. | ANDA077184 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 63304-497-01 | Sun Pharmaceutical Industries, Inc. | ANDA040826 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 63304-497-69 | Sun Pharmaceutical Industries, Inc. | ANDA040826 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; ASPIRIN; DIPHENHYDRAMINE CITRATE | 49467-230-10 | Sunascen Therapeutics LLC | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 49348-924-10 | Sunmark | ANDA076200 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 49348-921-10 | Sunmark | ANDA076200 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 49348-924-09 | Sunmark | ANDA076200 | HUMAN OTC DRUG | ANDA |
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