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; ACETAMINOPHEN; DOXYLAMINE SUCCINATE | 79481-8999-0 | Meijer, Inc. | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 79481-0184-8 | MEIJER, INC. | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 79481-0503-0 | Meijer, Inc. | ANDA214836 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 41250-278-08 | MEIJER, INC. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 54473-304-50 | Melaleuca, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 54473-098-04 | Melaleuca, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 54473-305-50 | Melaleuca, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 54473-304-01 | Melaleuca, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE | 53145-320-06 | Menper Distributors Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 53145-420-30 | Menper Distributors Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE | 53145-320-02 | Menper Distributors Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 53145-053-03 | Menper Distributors, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 58657-525-16 | 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 | 58657-524-04 | 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; TRAMADOL HYDROCHLORIDE | 42571-119-90 | Micro Labs Limited | ANDA201952 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE | 42571-119-32 | Micro Labs Limited | ANDA201952 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE | 42571-119-23 | Micro Labs Limited | ANDA201952 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE | 42571-119-01 | Micro Labs Limited | ANDA201952 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE | 42571-119-05 | Micro Labs Limited | ANDA201952 | HUMAN PRESCRIPTION DRUG | ANDA |
CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 76095-010-20 | MIDWAY IMPORTING INC. | M012 | HUMAN OTC DRUG | OTC monograph final |
CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 76095-010-02 | MIDWAY IMPORTING INC. | M012 | HUMAN OTC DRUG | OTC monograph final |
CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 76095-010-01 | MIDWAY IMPORTING INC. | M012 | HUMAN OTC DRUG | OTC monograph final |
CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 76095-010-10 | MIDWAY IMPORTING INC. | M012 | HUMAN OTC DRUG | OTC monograph final |
CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 76095-010-04 | MIDWAY IMPORTING INC. | M012 | HUMAN OTC DRUG | OTC monograph final |
CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 76095-010-50 | MIDWAY IMPORTING INC. | M012 | HUMAN OTC DRUG | OTC monograph final |
CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN | 76095-011-20 | Midway Importing, Inc. | part341 | HUMAN OTC DRUG | OTC monograph final |
CAFFEINE; BUTALBITAL; ACETAMINOPHEN | 46672-053-10 | Mikart, LLC | ANDA089175 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; BUTALBITAL; ACETAMINOPHEN | 46672-053-50 | Mikart, LLC | ANDA089175 | HUMAN PRESCRIPTION DRUG | ANDA |
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