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 | 21695-775-72 | Rebel Distributors Corp. | ANDA040556 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 21695-816-16 | Rebel Distributors Corp. | ANDA040182 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; CAFFEINE; ACETAMINOPHEN | 21695-843-60 | Rebel Distributors Corp. | ANDA040496 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 21695-924-40 | Rebel Distributors Corp. | ANDA040676 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 21695-987-15 | Rebel Distributors Corp. | ANDA040813 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 21695-987-30 | Rebel Distributors Corp. | ANDA040813 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 21695-987-60 | Rebel Distributors Corp. | ANDA040813 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 21695-987-72 | Rebel Distributors Corp. | ANDA040813 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 21695-987-90 | Rebel Distributors Corp. | ANDA040813 | HUMAN PRESCRIPTION DRUG | ANDA |
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 |
CHLOPHEDIANOL HYDROCHLORIDE; ACETAMINOPHEN; PYRILAMINE MALEATE | 23359-033-16 | Centurion Labs, LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 24201-100-24 | Hikma Pharmaceuticals USA Inc. | ANDA202605 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 24201-110-24 | Hikma Pharmaceuticals USA Inc. | ANDA202605 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 24286-1550-4 | DLC Laboratories, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 24385-005-30 | Amerisource Bergen | part341 | HUMAN OTC DRUG | OTC monograph final |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 24385-005-34 | Amerisource Bergen | part341 | HUMAN OTC DRUG | OTC monograph final |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 24385-005-38 | Amerisource Bergen | part341 | HUMAN OTC DRUG | OTC monograph final |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 24385-005-40 | Amerisource Bergen | part341 | HUMAN OTC DRUG | OTC monograph final |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 24385-036-62 | Amerisource Bergen | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN | 24385-066-62 | AmerisourceBergen Drug Corporation | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 24385-145-71 | Amerisource Bergen | part343 | HUMAN OTC DRUG | OTC monograph not final |
CAFFEINE; ASPIRIN; ACETAMINOPHEN | 24385-365-71 | Amerisource Bergen | ANDA075794 | HUMAN OTC DRUG | ANDA |
CAFFEINE; ASPIRIN; ACETAMINOPHEN | 24385-365-78 | Amerisource Bergen | ANDA075794 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 24385-484-14 | Amerisource Bergen | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 24385-484-47 | Amerisource Bergen | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 24385-484-71 | Amerisource Bergen | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 24385-484-76 | Amerisource Bergen | part343 | HUMAN OTC DRUG | OTC monograph not final |
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