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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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DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-21 | 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 | 0573-0167-26 | 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 | 0573-0167-43 | 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 | 0573-0167-55 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-56 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0168-20 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0168-30 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0168-40 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-02 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-08 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-11 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-13 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-17 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-19 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-20 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-22 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-30 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-31 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-40 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-43 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-49 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-51 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-52 | Haleon US Holdings LLC | NDA020402 | 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 | 0573-0169-89 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0170-01 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
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