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; PHENYLEPHRINE HYDROCHLORIDE | 0573-0199-01 | Haleon US Holdings LLC | NDA022565 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 66220-284-22 | Cumberland Pharmaceuticals Inc. | NDA022348 | HUMAN PRESCRIPTION DRUG | NDA |
ACETAMINOPHEN; IBUPROFEN | 67751-211-02 | Navajo Manufacturing Company Inc. | NDA211733 | HUMAN OTC DRUG | NDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 29485-6644-2 | Lil Drug Store Products, Inc | NDA021394 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-05 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-65 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0174-30 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; IBUPROFEN | 72260-129-01 | AFT Pharmaceuticals Ltd | NDA209471 | HUMAN PRESCRIPTION DRUG | NDA |
PHENYLEPHRINE HYDROCHLORIDE; IBUPROFEN | 52904-782-04 | Select Corporation | NDA022565 | HUMAN OTC DRUG | NDA |
IBUPROFEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 0573-0196-01 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-76 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-86 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-31 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-55 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0160-40 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-198-52 | Johnson & Johnson Consumer Inc. | NDA020603 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-13 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0168-20 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0154-98 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-89 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0191-20 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
IBUPROFEN; FAMOTIDINE | 75987-010-72 | Horizon Therapeutics USA, Inc. | NDA022519 | HUMAN PRESCRIPTION DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 67751-149-01 | Navajo Manufacturing Company Inc. | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 66715-6500-2 | Lil' Drug Store Products, Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 67751-147-01 | Navajo Manufacturing Company Inc. | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0165-20 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 29485-1465-4 | Lil' Drug Store Products, Inc. | NDA019012 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-55 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-14 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0191-50 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
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