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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PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE | 37808-286-01 | HEB | part341 | HUMAN OTC DRUG | OTC monograph final |
CHLORPHENIRAMINE MALEATE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 37808-628-02 | HEB | part341 | HUMAN OTC DRUG | OTC monograph final |
GUAIFENESIN; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE | 37808-497-04 | HEB | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE | 37808-095-16 | H-E-B | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 37808-333-01 | H-E-B | ANDA076200 | HUMAN OTC DRUG | ANDA |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DOXYLAMINE SUCCINATE | 37808-191-48 | H-E-B | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 37808-093-16 | H-E-B | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 37808-333-50 | H-E-B | ANDA076200 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 49260-710-50 | Help Remedies, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 49260-710-02 | Help Remedies, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 49260-710-20 | Help Remedies, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 0404-0716-99 | Henry Schein, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 0404-0714-13 | Henry Schein, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 0404-0716-13 | Henry Schein, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 0404-0714-99 | Henry Schein, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 23155-202-01 | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA207035 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 23155-202-18 | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA207035 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 23155-202-64 | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA207035 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 23155-202-65 | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA207035 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 51662-1540-3 | HF Acquisition Co LLC, DBA HealthFirst | ANDA210969 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 51662-1424-1 | HF Acquisition Co LLC, DBA HealthFirst | NDA022450 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN | 51662-1274-2 | HF Acquisition Co LLC, DBA HealthFirst | 505G(a)(3) | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 51662-1540-2 | HF Acquisition Co LLC, DBA HealthFirst | ANDA210969 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 24201-110-24 | Hikma Pharmaceuticals USA Inc. | ANDA202605 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 24201-100-24 | Hikma Pharmaceuticals USA Inc. | ANDA202605 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE; CAFFEINE; BUTALBITAL | 0054-0650-25 | Hikma Pharmaceuticals USA Inc. | ANDA215138 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 0143-9386-10 | Hikma Pharmaceuticals USA Inc. | NDA206968 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN; ACETAMINOPHEN | 0143-9150-10 | Hikma Pharmaceuticals USA Inc. | NDA215320 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN | 0143-9386-01 | Hikma Pharmaceuticals USA Inc. | NDA206968 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN; CAFFEINE; CODEINE PHOSPHATE; BUTALBITAL | 0054-3000-01 | Hikma Pharmaceuticals USA Inc. | ANDA215138 | HUMAN PRESCRIPTION DRUG | ANDA |
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