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 | 0573-0170-30 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-198-52 | Johnson & Johnson Consumer Inc. | NDA020603 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-198-50 | Johnson & Johnson Consumer Inc. | NDA020603 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-198-51 | Johnson & Johnson Consumer Inc. | NDA020603 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-100-18 | Johnson & Johnson Consumer Inc. | NDA020603 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0191-75 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0191-20 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0191-22 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0191-50 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 71205-425-24 | Proficient Rx LP | NDA020944 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0179-20 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020944 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0184-16 | Haleon US Holdings LLC | NDA021374 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0184-32 | Haleon US Holdings LLC | NDA021374 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-55 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-25 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-42 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-19 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-10 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-56 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-21 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-18 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-26 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-44 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-43 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-20 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-43 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 66715-9733-8 | Lil' Drug Store Products, Inc. | NDA021394 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 29485-7008-3 | Lil Drug Store Products, Inc | NDA021394 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-33 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-04 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
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