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 | 68998-001-02 | Marc Glassman, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 68998-004-04 | Marc Glassman, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 68998-004-06 | Marc Glassman, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 68998-070-03 | MARC GLASSMAN, INC. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 68998-071-03 | MARC GLASSMAN, INC. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68998-092-01 | Marc Glassman, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 68998-095-02 | Marc Glassman, Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68998-098-02 | Marc Glassman, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 68998-104-04 | MARC GLASSMAN, INC. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 68998-104-06 | MARC GLASSMAN, INC. | part343 | HUMAN OTC DRUG | OTC monograph not final |
GUAIFENESIN; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 68998-119-05 | Marc Glassman, Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
GUAIFENESIN; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE | 68998-136-02 | Marc Glassman, Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE | 68998-138-05 | Marc Glassman, Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE | 68998-139-02 | Marc Glassman, Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
GUAIFENESIN; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE | 68998-163-05 | Marc Glassman, Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68998-170-03 | Marc Glassman, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE | 68998-175-02 | Marc Glassman, Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 68998-195-02 | MARC GLASSMAN, INC. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68998-198-02 | MARC GLASSMAN, INC. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN | 68998-219-05 | MARC GLASSMAN, INC. | part341 | HUMAN OTC DRUG | OTC monograph final |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 68998-220-06 | MARC GLASSMAN, INC. | part341 | HUMAN OTC DRUG | OTC monograph final |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE | 68998-228-02 | MARC GLASSMAN, INC. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE | 68998-238-05 | MARC GLASSMAN, INC. | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; GUAIFENESIN | 68998-263-05 | MARC GLASSMAN, INC. | part341 | HUMAN OTC DRUG | OTC monograph final |
GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 68998-275-02 | MARC GLASSMAN, INC. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68998-300-03 | MARC GLASSMAN, INC. | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 68998-301-01 | MARC GLASSMAN, INC. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 68998-323-05 | MARC GLASSMAN, INC. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 68998-392-01 | MARC GLASSMAN, INC. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 68998-401-03 | MARC GLASSMAN, INC. | ANDA211544 | HUMAN OTC DRUG | ANDA |
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