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 | 0573-0149-91 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0150-30 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-01 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0151-20 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 66715-9752-3 | Lil Drug Store Products, Inc | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 52904-793-04 | Select Corporation | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0149-04 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 66715-9700-1 | Lil' Drug Store Products, Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-100-18 | Johnson & Johnson Consumer Inc. | NDA020603 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0151-10 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0149-66 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0154-59 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-148-02 | Navajo Manufacturing Company Inc. | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-198-50 | Johnson & Johnson Consumer Inc. | NDA020603 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0160-41 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 66220-284-11 | Cumberland Pharmaceuticals Inc. | NDA022348 | HUMAN PRESCRIPTION DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 67751-149-03 | Navajo Manufacturing Company Inc. | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0161-35 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0154-89 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 29485-7006-3 | Lil' Drug Store Products, Inc. | NDA019012 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-04 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-40 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 0573-0196-02 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0151-30 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0160-42 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0151-21 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 0573-0190-02 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-198-51 | Johnson & Johnson Consumer Inc. | NDA020603 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 66220-287-11 | Cumberland Pharmaceuticals Inc. | NDA022348 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-05 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
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