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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CAFFEINE; ACETAMINOPHEN; ASPIRIN | 30142-896-78 | Kroger Company | ANDA075794 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 30142-818-26 | Kroger Company | part343 | HUMAN OTC DRUG | OTC monograph not final |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; DOXYLAMINE SUCCINATE | 30142-459-40 | Kroger Company | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 41226-340-01 | KROGER COMPANY | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; DOXYLAMINE SUCCINATE | 30142-629-12 | KROGER COMPANY | part341 | HUMAN OTC DRUG | OTC monograph final |
GUAIFENESIN; ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 30142-828-09 | Kroger Company | M012 | HUMAN OTC DRUG | OTC Monograph Drug |
DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; DOXYLAMINE SUCCINATE | 30142-459-38 | Kroger Company | part341 | HUMAN OTC DRUG | OTC monograph final |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 30142-113-07 | Kroger Company | part341 | HUMAN OTC DRUG | OTC MONOGRAPH FINAL |
PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 30142-964-91 | Kroger Company | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 30142-507-62 | Kroger Company | part343 | HUMAN OTC DRUG | OTC monograph not final |
BENZHYDROCODONE HYDROCHLORIDE; ACETAMINOPHEN | 10702-344-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
BENZHYDROCODONE HYDROCHLORIDE; ACETAMINOPHEN | 10702-342-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN; OXYCODONE | 10702-186-10 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; CAFFEINE; ACETAMINOPHEN | 10702-253-50 | KVK-Tech, Inc. | ANDA211106 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE | 10702-186-01 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 10702-189-50 | KVK-Tech, Inc. | ANDA209037 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 10702-190-10 | KVK-Tech, Inc. | ANDA209037 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE; ACETAMINOPHEN | 10702-187-50 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE; ACETAMINOPHEN | 10702-185-10 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE; ACETAMINOPHEN | 10702-187-10 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; CAFFEINE; ACETAMINOPHEN | 10702-253-01 | KVK-Tech, Inc. | ANDA211106 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE; ACETAMINOPHEN | 10702-185-50 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE | 10702-186-50 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; BENZHYDROCODONE HYDROCHLORIDE | 10702-340-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 10702-238-50 | KVK-Tech, Inc. | ANDA211499 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 10702-191-10 | KVK-Tech, Inc. | ANDA209037 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 10702-193-03 | KVK-Tech, Inc. | ANDA209036 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 10702-191-01 | KVK-Tech, Inc. | ANDA209037 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE | 10702-184-10 | KVK-Tech, Inc. | ANDA210644 | HUMAN PRESCRIPTION DRUG | ANDA |
BENZHYDROCODONE HYDROCHLORIDE; ACETAMINOPHEN | 10702-343-01 | KVK-Tech, Inc. | NDA208653 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
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