FDA Application
-
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 |
---|---|---|---|---|---|
GLUCOSAMINE SULFATE; IBUPROFEN; CHONDROITIN SULFATE (BOVINE) | 61841-152-72 | Bayer HealthCare LLC. | HUMAN OTC DRUG | Export only | |
IBUPROFEN | 62207-365-27 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-366-66 | Granules India Limited | BULK INGREDIENT | Export only | |
GLUCOSAMINE SULFATE; IBUPROFEN; CHONDROITIN SULFATE (BOVINE) | 61841-152-12 | Bayer HealthCare LLC. | HUMAN OTC DRUG | Export only | |
IBUPROFEN | 62207-365-26 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-311-19 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-366-25 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-366-80 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-366-68 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-365-68 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-303-04 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-366-26 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-366-67 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-365-67 | Granules India Limited | BULK INGREDIENT | Export only | |
IBUPROFEN | 62207-366-27 | Granules India Limited | BULK INGREDIENT | Export only | |
CHONDROITIN SULFATE (BOVINE); IBUPROFEN; GLUCOSAMINE SULFATE | 10267-3479-5 | Contract Pharmacal Corp. | HUMAN OTC DRUG | Export only | |
IBUPROFEN | 0573-0160-25 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0230-20 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-1769-20 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 0573-0196-10 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0166-51 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-603-04 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN; ACETAMINOPHEN | 0573-0147-36 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
IBUPROFEN; DIPHENHYDRAMINE CITRATE | 66715-9733-8 | Lil' Drug Store Products, Inc. | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-20 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; IBUPROFEN | 0573-0145-72 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-1769-80 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0165-30 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 29485-7008-3 | Lil Drug Store Products, Inc | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 73097-008-50 | Savings Distributors LLC | NDA019012 | HUMAN OTC DRUG | NDA |
-