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 | 51013-402-25 | PuraCap Pharmaceutical LLC | part343 | HUMAN OTC DRUG | OTC monograph not final |
PHENYLEPHRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE; ACETAMINOPHEN; DOXYLAMINE SUCCINATE | 51013-168-08 | PuraCap Pharmaceutical LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE | 51013-185-14 | PuraCap Pharmaceutical LLC | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 51013-173-43 | PuraCap Pharmaceutical LLC | part343 | HUMAN OTC DRUG | OTC monograph not final |
DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE | 51013-110-04 | PuraCap Pharmaceutical LLC. | part341 | HUMAN OTC DRUG | OTC monograph final |
ACETAMINOPHEN | 83474-001-04 | Puro Pharma Inc. | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
CAFFEINE; BUTALBITAL; ACETAMINOPHEN | 70752-144-10 | QUAGEN PHARMACEUTICALS LLC | ANDA214288 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; ACETAMINOPHEN | 70752-148-14 | QUAGEN PHARMACEUTICALS LLC | ANDA214291 | HUMAN PRESCRIPTION DRUG | ANDA |
BUTALBITAL; ACETAMINOPHEN | 70752-148-10 | QUAGEN PHARMACEUTICALS LLC | ANDA214291 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; BUTALBITAL | 70752-147-10 | QUAGEN PHARMACEUTICALS LLC | ANDA214305 | HUMAN PRESCRIPTION DRUG | ANDA |
CAFFEINE; BUTALBITAL; ACETAMINOPHEN | 70752-144-14 | QUAGEN PHARMACEUTICALS LLC | ANDA214288 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CAFFEINE; BUTALBITAL | 70752-142-10 | QUAGEN PHARMACEUTICALS LLC | ANDA214287 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; BUTALBITAL | 70752-147-14 | QUAGEN PHARMACEUTICALS LLC | ANDA214305 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; CAFFEINE; BUTALBITAL | 70752-142-14 | QUAGEN PHARMACEUTICALS LLC | ANDA214287 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 55700-498-28 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 55700-498-40 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 55700-496-60 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 55700-498-05 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 55700-498-21 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 49999-852-00 | Quality Care products LLC | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 55700-496-90 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 55700-498-15 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 55700-497-60 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 55700-498-30 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 55700-496-01 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 55700-498-14 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 55700-497-28 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 49999-852-90 | Quality Care products LLC | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 49999-852-30 | Quality Care products LLC | ANDA087463 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 55700-498-90 | Quality Care Products LLC | ANDA201972 | HUMAN PRESCRIPTION DRUG | ANDA |
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