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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OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 0527-1671-01 | Lannett Company, Inc. | ANDA207333 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 0527-1651-01 | Lannett Company, Inc. | ANDA207172 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 0527-1648-01 | Lannett Company, Inc. | ANDA207171 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; BUTALBITAL; ACETAMINOPHEN | 0527-4095-37 | Lannett Company, Inc. | ANDA212082 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; ACETAMINOPHEN; BUTALBITAL | 0527-1695-01 | Lannett Company, Inc. | ANDA200243 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 0527-1648-05 | Lannett Company, Inc. | ANDA207171 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 0527-1646-01 | Lannett Company, Inc. | ANDA207171 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 54838-144-70 | Lannett Company, Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 0527-1646-05 | Lannett Company, Inc. | ANDA207171 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 0527-1647-05 | 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 | 0527-1650-01 | Lannett Company, Inc. | ANDA207172 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; ACETAMINOPHEN; BUTALBITAL | 0527-1695-05 | Lannett Company, Inc. | ANDA200243 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 0527-1647-01 | Lannett Company, Inc. | ANDA207171 | 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 | 0527-1671-05 | Lannett Company, Inc. | ANDA207333 | HUMAN PRESCRIPTION DRUG | ANDA |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 0527-1650-05 | Lannett Company, Inc. | ANDA207172 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; ACETAMINOPHEN | 68047-721-30 | Larken Laboratories, Inc. | ANDA203484 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; BUTALBITAL | 68047-752-01 | Larken Laboratories, Inc. | ANDA203484 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; ACETAMINOPHEN | 68047-721-01 | Larken Laboratories, Inc. | ANDA203484 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; BUTALBITAL | 68047-753-01 | Larken Laboratories, Inc. | ANDA203484 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; BUTALBITAL | 68047-753-30 | Larken Laboratories, Inc. | ANDA203484 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; BUTALBITAL | 68047-752-30 | Larken Laboratories, Inc. | ANDA203484 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 70000-0626-1 | LEADER/ Cardinal Health 110, Inc | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 70000-0627-2 | LEADER/ Cardinal Health 110, Inc | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 70000-0627-3 | LEADER/ Cardinal Health 110, Inc | ANDA211544 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 70000-0627-1 | LEADER/ Cardinal Health 110, Inc | ANDA211544 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; ACETAMINOPHEN | 70000-0622-1 | LEADER/ Cardinal Health 110, Inc. | ANDA216592 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; ACETAMINOPHEN | 70000-0622-2 | LEADER/ Cardinal Health 110, Inc. | ANDA216592 | HUMAN OTC DRUG | ANDA |
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