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 |
---|---|---|---|---|---|
ACETAMINOPHEN; HYDROCODONE BITARTRATE | 43386-358-10 | Lupin Pharmaceuticals,Inc. | ANDA206245 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 43386-490-01 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 43386-490-05 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 43386-490-10 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43386-491-01 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43386-491-05 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43386-491-10 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43386-492-01 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43386-492-05 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43386-492-10 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 43386-493-01 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 43386-493-05 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 43386-493-10 | Lupin Pharmaceuticals,Inc. | ANDA204407 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; PENTAZOCINE HYDROCHLORIDE | 43386-670-01 | GAVIS Pharmaceuticals, LLC | ANDA076202 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 43459-0152-6 | Etex Pharm Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 43459-0153-6 | Etex Pharm Inc. | part343 | HUMAN OTC DRUG | OTC monograph not final |
CAFFEINE; BUTALBITAL; ACETAMINOPHEN | 43547-686-10 | SOLCO HEALTHCARE US, LLC | ANDA214087 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43598-546-01 | Dr. ReddyÂ’s Laboratories Inc. | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43598-546-05 | Dr. ReddyÂ’s Laboratories Inc. | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43598-547-01 | Dr. ReddyÂ’s Laboratories Inc. | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 43598-547-05 | Dr. ReddyÂ’s Laboratories Inc. | ANDA207510 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 44224-0016-1 | Unifirst First Aid Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
ACETAMINOPHEN | 44224-0016-2 | Unifirst First Aid Corporation | part343 | HUMAN OTC DRUG | OTC monograph not final |
DIPHENHYDRAMINE HYDROCHLORIDE; BENZALKONIUM CHLORIDE; NEOMYCIN SULFATE; ASPIRIN; POVIDONE-IODINE; IBUPROFEN; ACETAMINOPHEN; POLYMYXIN B SULFATE; BACITRACIN ZINC | 44224-0118-1 | Tender Corporation DBA Adventure Ready Brands | part333A | HUMAN OTC DRUG | OTC monograph final |
ALCOHOL; ACETAMINOPHEN; POLYMYXIN B SULFATE; BENZALKONIUM CHLORIDE; BENZOCAINE; IBUPROFEN; NEOMYCIN SULFATE; BACITRACIN ZINC | 44224-0699-5 | Tender Corporation DBA Adventure Ready Brands | part348 | HUMAN OTC DRUG | OTC monograph final |
NEOMYCIN SULFATE; BENZALKONIUM CHLORIDE; IBUPROFEN; ALCOHOL; ACETAMINOPHEN; BACITRACIN ZINC; POLYMYXIN B SULFATE; BENZOCAINE | 44224-0999-5 | Tender Corporation DBA Adventure Ready Brands | part348 | HUMAN OTC DRUG | OTC monograph final |
BENZALKONIUM CHLORIDE; BENZOCAINE; ALCOHOL; BACITRACIN ZINC; ACETAMINOPHEN; LIDOCAINE; NEOMYCIN SULFATE; IBUPROFEN; POLYMYXIN B SULFATE | 44224-1999-6 | Tender Corporation DBA Adventure Ready Brands | part348 | HUMAN OTC DRUG | OTC monograph final |
ASPIRIN; BENZALKONIUM CHLORIDE; DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN; BENZOCAINE; NEOMYCIN SULFATE; ALCOHOL; BACITRACIN ZINC; POLYMYXIN B SULFATE; ACETAMINOPHEN | 44224-2000-1 | Tender Corporation DBA Adventure Ready Brands | part333B | HUMAN OTC DRUG | OTC monograph not final |
BENZALKONIUM CHLORIDE; ACETAMINOPHEN; IBUPROFEN; POLYMYXIN B SULFATE; ASPIRIN; BACITRACIN ZINC; BENZOCAINE; ALCOHOL; NEOMYCIN SULFATE | 44224-2500-1 | Tender Corporation DBA Adventure Ready Brands | part333B | HUMAN OTC DRUG | OTC monograph not final |
LIDOCAINE HYDROCHLORIDE; ACETAMINOPHEN; BENZALKONIUM CHLORIDE; ASPIRIN; AMMONIA; IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE | 44224-2999-0 | Tender Corporation | part333A | HUMAN OTC DRUG | OTC monograph not final |
-