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; IBUPROFEN | 58602-895-62 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-65 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-73 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-78 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-79 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-80 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-82 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-84 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-85 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-88 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-94 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-95 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-96 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-99 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 58657-524-04 | Method Pharmaceuticals, LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 58657-524-16 | Method Pharmaceuticals, LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 58657-525-04 | Method Pharmaceuticals, LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 58657-525-16 | Method Pharmaceuticals, LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 58805-002-08 | Agile Pharmachem | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 58805-002-14 | Agile Pharmachem | part341 | HUMAN OTC DRUG | OTC monograph final |
DOXYLAMINE SUCCINATE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 58805-003-04 | Agile Pharmachem | part341 | HUMAN OTC DRUG | OTC monograph final |
DOXYLAMINE SUCCINATE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 58805-003-14 | Agile Pharmachem | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 58805-004-12 | AGILE PHARMACHEM | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 58805-004-16 | AGILE PHARMACHEM | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 58805-004-18 | AGILE PHARMACHEM | part341 | HUMAN OTC DRUG | OTC monograph final |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 58933-539-01 | Procter & Gamble Manufacturing México, S. de R.L. de C.V. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 58933-539-09 | Procter & Gamble Manufacturing México, S. de R.L. de C.V. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE | 58933-542-16 | Procter & Gamble Manufactura S de RL de CV | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 58933-550-01 | Procter & Gamble Manufactura S de RL de CV | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 58933-550-08 | Procter & Gamble Manufactura S de RL de CV | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
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