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 | 67751-146-01 | Navajo Manufacturing Company Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0154-17 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-20 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0171-03 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
PHENYLEPHRINE HYDROCHLORIDE; IBUPROFEN | 67751-150-02 | Navajo Manufacturing Company Inc. | NDA022565 | HUMAN OTC DRUG | NDA |
IBUPROFEN LYSINE | 55292-122-52 | Recordati Rare Diseases Inc. | NDA021903 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN | 0573-0169-49 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
PHENYLEPHRINE HYDROCHLORIDE; IBUPROFEN | 52904-782-03 | Select Corporation | NDA022565 | HUMAN OTC DRUG | NDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 66715-6433-2 | Lil' Drug Store Products, Inc. | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-22 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-32 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0165-25 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 52904-793-05 | Select Corporation | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 66715-6434-2 | Lil' Drug Store Products, Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-19 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0179-20 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020944 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 29485-6552-4 | Lil' Drug Store Products, Inc. | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 29485-2893-4 | Lil' Drug Store Products, Inc. | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN; ACETAMINOPHEN | 0573-0147-93 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 67751-149-02 | Navajo Manufacturing Company Inc. | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0170-32 | Haleon US Holdings LLC | NDA020589 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0154-21 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-604-04 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 66715-5803-0 | Lil' Drug Store Products, Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 52904-793-25 | Select Corporation | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-601-08 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-601-21 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN | 0573-0167-10 | Haleon US Holdings LLC | NDA021393 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 66220-287-24 | Cumberland Pharmaceuticals Inc. | NDA022348 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN | 0573-0169-11 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
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