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; HYDROCODONE BITARTRATE | 0527-1648-05 | Lannett Company, Inc. | ANDA207171 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 0527-1649-01 | Lannett Company, Inc. | ANDA207172 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 0527-1649-05 | Lannett Company, Inc. | ANDA207172 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 0527-1650-01 | Lannett Company, Inc. | ANDA207172 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 0527-1650-05 | Lannett Company, Inc. | ANDA207172 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 0527-1651-01 | Lannett Company, Inc. | ANDA207172 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 0527-1651-05 | Lannett Company, Inc. | ANDA207172 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 0527-1669-01 | Lannett Company, Inc. | ANDA207333 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 0527-1669-05 | Lannett Company, Inc. | ANDA207333 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 0527-1671-01 | Lannett Company, Inc. | ANDA207333 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 0527-1671-05 | Lannett Company, Inc. | ANDA207333 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; ACETAMINOPHEN; BUTALBITAL | 0527-1695-01 | Lannett Company, Inc. | ANDA200243 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; ACETAMINOPHEN; BUTALBITAL | 0527-1695-05 | Lannett Company, Inc. | ANDA200243 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; CAFFEINE; ACETAMINOPHEN | 0527-4094-37 | Lannett Company, Inc. | ANDA212083 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; BUTALBITAL; ACETAMINOPHEN | 0527-4095-37 | Lannett Company, Inc. | ANDA212082 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 0536-1164-01 | Rugby Laboratories | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 0536-1172-01 | Rugby Laboratories | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 0536-1172-10 | Rugby Laboratories | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 0536-1212-77 | Rugby Laboratories | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 0536-1289-35 | Rugby Laboratories | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 0536-1292-29 | Rugby Laboratories | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 0536-1321-97 | Rugby Laboratories | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; ASPIRIN; CAFFEINE | 0536-1326-01 | Rugby Laboratories | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 0536-1327-01 | RUGBY LABORATORIES | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 0536-1327-06 | RUGBY LABORATORIES | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 0536-1327-10 | RUGBY LABORATORIES | part343 | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN; ACETAMINOPHEN | 0536-1376-36 | RUGBY LABORATORIES | ANDA216592 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 0536-1426-77 | Rugby Laboratories | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
IBUPROFEN; ACETAMINOPHEN | 0573-0145-02 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
IBUPROFEN; ACETAMINOPHEN | 0573-0145-18 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
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