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NDC Search Results on Active Ingredient: ibuprofen
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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IBUPROFEN | 0573-0165-41 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-09 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0151-13 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0149-13 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0160-30 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-30 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-52 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-10 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 0573-0196-20 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0180-21 | Haleon US Holdings LLC | NDA019771 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-91 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-88 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-08 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-42 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-1769-13 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0160-31 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-91 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-04 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-43 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0150-40 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-1174-12 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0150-41 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0184-16 | Haleon US Holdings LLC | NDA021374 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-03 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-1711-14 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-20 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; IBUPROFEN | 0573-0145-02 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
PHENYLEPHRINE HYDROCHLORIDE; CHLORPHENIRAMINE MALEATE; IBUPROFEN | 0573-2161-03 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-1769-89 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-44 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
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