FDA Application
-
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 |
---|---|---|---|---|---|
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65841-758-10 | Zydus Lifesciences Limited | ANDA090460 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65862-922-01 | Aurobindo Pharma Limited | ANDA207152 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65862-922-05 | Aurobindo Pharma Limited | ANDA207152 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65862-922-10 | Aurobindo Pharma Limited | ANDA207152 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65862-922-30 | Aurobindo Pharma Limited | ANDA207152 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65862-922-78 | Aurobindo Pharma Limited | ANDA207152 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65862-922-99 | Aurobindo Pharma Limited | ANDA207152 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE | 65923-627-04 | United Exchange Corp. | part341 | HUMAN OTC DRUG | OTC monograph final |
DOXYLAMINE SUCCINATE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN | 65923-629-04 | United Exchange Corp. | part341 | HUMAN OTC DRUG | OTC monograph final |
DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; ACETAMINOPHEN | 65923-630-04 | United Exchange Corp. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 66007-145-01 | Capricorn Pharma Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 66007-145-02 | Capricorn Pharma Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 66267-319-30 | NuCare Pharmaceuticals,Inc. | ANDA201013 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 66267-858-06 | NuCare Pharmaceuticals,Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 66336-012-14 | Dispensing Solutions, Inc. | ANDA040144 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 66336-012-15 | Dispensing Solutions, Inc. | ANDA040144 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 66336-012-20 | Dispensing Solutions, Inc. | ANDA040144 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 66336-012-30 | Dispensing Solutions, Inc. | ANDA040144 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 66336-012-40 | Dispensing Solutions, Inc. | ANDA040144 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 66336-012-60 | Dispensing Solutions, Inc. | ANDA040144 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 66336-012-62 | Dispensing Solutions, Inc. | ANDA040144 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 66336-012-90 | Dispensing Solutions, Inc. | ANDA040144 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 66336-012-94 | Dispensing Solutions, Inc. | ANDA040144 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 66336-019-20 | Dispensing Solutions, Inc. | ANDA040144 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 66336-019-30 | Dispensing Solutions, Inc. | ANDA040144 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 66336-019-60 | Dispensing Solutions, Inc. | ANDA040144 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 66336-059-06 | Dispensing Solutions, Inc. | ANDA089805 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 66336-059-10 | Dispensing Solutions, Inc. | ANDA089805 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 66336-059-12 | Dispensing Solutions, Inc. | ANDA089805 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 66336-059-15 | Dispensing Solutions, Inc. | ANDA089805 | HUMAN PRESCRIPTION DRUG | ANDA |
-