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 | 17856-1986-3 | Atlantic Biologicals Corps | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
ACETAMINOPHEN | 17856-1986-2 | Atlantic Biologicals Corps | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
HYDROCODONE BITARTRATE; ACETAMINOPHEN | 17856-0450-1 | Atlantic Biologicals Corps | ANDA040881 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 17856-0985-4 | Atlantic Biologicals Corps | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
ACETAMINOPHEN | 17856-0985-8 | Atlantic Biologicals Corps | part343 | HUMAN OTC DRUG | OTC MONOGRAPH NOT FINAL |
ACETAMINOPHEN; BUTALBITAL; CAFFEINE | 59702-661-12 | Atley Pharmaceuticals, Inc. | ANDA040885 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; BUTALBITAL; CAFFEINE | 59702-661-01 | Atley Pharmaceuticals, Inc. | ANDA040885 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN | 71009-109-01 | Aurex Laboratories Limited Liability Company | part343 | HUMAN OTC DRUG | OTC monograph not final |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65862-922-99 | Aurobindo Pharma Limited | ANDA207152 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65862-922-30 | Aurobindo Pharma Limited | ANDA207152 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65862-922-01 | Aurobindo Pharma Limited | ANDA207152 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65862-922-05 | Aurobindo Pharma Limited | ANDA207152 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65862-922-78 | Aurobindo Pharma Limited | ANDA207152 | HUMAN PRESCRIPTION DRUG | ANDA |
TRAMADOL HYDROCHLORIDE; ACETAMINOPHEN | 65862-922-10 | Aurobindo Pharma Limited | ANDA207152 | HUMAN PRESCRIPTION DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-88 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-893-49 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 58602-760-73 | Aurohealth LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 58602-771-64 | Aurohealth LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; IBUPROFEN | 58602-895-85 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE | 58602-760-14 | Aurohealth LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN | 58602-730-07 | Aurohealth LLC | ANDA207229 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 58602-730-28 | Aurohealth LLC | ANDA207229 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 58602-873-40 | Aurohealth LLC | ANDA207229 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 58602-776-88 | Aurohealth LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; IBUPROFEN | 58602-895-95 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-895-35 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN; IBUPROFEN | 58602-893-80 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 58602-755-40 | Aurohealth LLC | M013 | HUMAN OTC DRUG | OTC Monograph Drug |
ACETAMINOPHEN; IBUPROFEN | 58602-893-11 | Aurohealth LLC | ANDA218359 | HUMAN OTC DRUG | ANDA |
ACETAMINOPHEN | 58602-873-36 | Aurohealth LLC | ANDA207229 | HUMAN OTC DRUG | ANDA |
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