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; OXYCODONE HYDROCHLORIDE | 63187-824-30 | Proficient Rx LP | ANDA201278 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 63187-824-60 | Proficient Rx LP | ANDA201278 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 63187-824-90 | Proficient Rx LP | ANDA201278 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 63187-838-12 | Proficient Rx LP | ANDA040148 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 63187-838-15 | Proficient Rx LP | ANDA040148 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 63187-838-20 | Proficient Rx LP | ANDA040148 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 63187-838-30 | Proficient Rx LP | ANDA040148 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 63187-838-60 | Proficient Rx LP | ANDA040148 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 63187-838-90 | Proficient Rx LP | ANDA040148 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; ACETAMINOPHEN; CAFFEINE | 63187-933-14 | Proficient Rx LP | ANDA200243 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; ACETAMINOPHEN; CAFFEINE | 63187-933-30 | Proficient Rx LP | ANDA200243 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; ACETAMINOPHEN; CAFFEINE | 63187-933-60 | Proficient Rx LP | ANDA200243 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; ACETAMINOPHEN; CAFFEINE | 63187-933-90 | Proficient Rx LP | ANDA200243 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 63187-968-30 | Proficient Rx LP | part343 | HUMAN OTC DRUG | OTC monograph not final |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 63187-984-10 | Proficient Rx LP | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 63187-984-12 | Proficient Rx LP | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 63187-984-15 | Proficient Rx LP | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 63187-984-30 | Proficient Rx LP | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 63187-984-60 | Proficient Rx LP | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 63304-497-01 | Sun Pharmaceutical Industries, Inc. | ANDA040826 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 63304-497-03 | Sun Pharmaceutical Industries, Inc. | ANDA040826 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 63304-497-05 | Sun Pharmaceutical Industries, Inc. | ANDA040826 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 63304-497-10 | Sun Pharmaceutical Industries, Inc. | ANDA040826 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 63304-497-11 | Sun Pharmaceutical Industries, Inc. | ANDA040826 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 63304-497-69 | Sun Pharmaceutical Industries, Inc. | ANDA040826 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 63304-561-01 | Sun Pharmaceutical Industries, Inc. | ANDA087083 | HUMAN PRESCRIPTION DRUG | ANDA |
CODEINE PHOSPHATE; ACETAMINOPHEN | 63304-561-05 | Sun Pharmaceutical Industries, Inc. | ANDA087083 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 63304-562-01 | Sun Pharmaceutical Industries, Inc. | ANDA085868 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 63304-562-05 | Sun Pharmaceutical Industries, Inc. | ANDA085868 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CODEINE PHOSPHATE | 63304-562-10 | Sun Pharmaceutical Industries, Inc. | ANDA085868 | HUMAN PRESCRIPTION DRUG | ANDA |
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