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 |
---|---|---|---|---|---|
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 | 0573-0160-41 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0154-89 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0165-42 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0151-12 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0161-65 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0154-16 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0160-25 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0166-51 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 73097-008-40 | Savings Distributors LLC | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 29485-7006-3 | Lil' Drug Store Products, Inc. | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-120-02 | Navajo Manufacturing Company Inc. | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-120-01 | Navajo Manufacturing Company Inc. | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 73097-008-50 | Savings Distributors LLC | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 73097-008-02 | Savings Distributors LLC | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 29485-1465-4 | Lil' Drug Store Products, Inc. | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 29485-6512-4 | Lil' Drug Store Products, Inc. | NDA019012 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 29485-7938-6 | Lil' Drug Store Products, Inc. | NDA019012 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0180-21 | Haleon US Holdings LLC | NDA019771 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0180-10 | Haleon US Holdings LLC | NDA019771 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0175-11 | Haleon US Holdings LLC | NDA020267 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-11 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 52904-793-25 | Select Corporation | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 29485-2893-4 | Lil' Drug Store Products, Inc. | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 29485-6552-4 | Lil' Drug Store Products, Inc. | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-49 | 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 | 0573-0169-51 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
-