FDA Application
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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; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 0573-0196-20 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-52 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 52904-794-01 | Wyeth Pharmaceuticals Company | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-148-01 | Navajo Manufacturing Company Inc. | NDA020402 | 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 | 0573-0191-22 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0180-21 | Haleon US Holdings LLC | NDA019771 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 71205-425-24 | Proficient Rx LP | NDA020944 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-184-01 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-10 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-1769-13 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 52904-791-25 | Wyeth Pharmaceuticals Company | NDA018989 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-42 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 29485-7088-4 | Lil Drug Store Products, Inc | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-08 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0150-41 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-1174-12 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-03 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0184-16 | Haleon US Holdings LLC | NDA021374 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-04 | Haleon US Holdings LLC | NDA201803 | 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 |
IBUPROFEN | 0573-1711-14 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 66715-6533-2 | Lil' Drug Store Products, Inc. | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-91 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0160-31 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 73097-008-50 | Savings Distributors LLC | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-02 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-20 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
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