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; PHENYLEPHRINE HYDROCHLORIDE | 0573-0199-11 | Haleon US Holdings LLC | NDA022565 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 29485-6939-3 | Lil' Drug Store Products, Inc. | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-601-20 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN; ACETAMINOPHEN | 0573-0147-91 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 52904-794-02 | Wyeth Pharmaceuticals Company | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 52904-786-50 | Wyeth Pharmaceuticals Company | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0154-35 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-1769-14 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-44 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-184-51 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
IBUPROFEN; ACETAMINOPHEN | 0573-0147-72 | Haleon US Holdings LLC | NDA211733 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0184-32 | Haleon US Holdings LLC | NDA021374 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0160-20 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-1769-89 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN; ACETAMINOPHEN | 0143-9150-01 | Hikma Pharmaceuticals USA Inc. | NDA215320 | HUMAN PRESCRIPTION DRUG | NDA |
PHENYLEPHRINE HYDROCHLORIDE; CHLORPHENIRAMINE MALEATE; IBUPROFEN | 0573-2161-03 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 66715-6452-2 | Lil Drug Store Products, Inc | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50269-157-02 | JC World Bell Wholesale Co., Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0160-17 | Haleon US Holdings LLC | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 52904-793-30 | Select Corporation | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 0573-0196-20 | Haleon US Holdings LLC | NDA022113 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0169-52 | Haleon US Holdings LLC | NDA020402 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 52904-794-01 | Wyeth Pharmaceuticals Company | NDA018989 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-148-01 | Navajo Manufacturing Company Inc. | NDA020402 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 0573-0164-91 | Haleon US Holdings LLC | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN SODIUM | 0573-0133-88 | Haleon US Holdings LLC | NDA201803 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0573-0191-22 | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC | NDA020812 | HUMAN OTC DRUG | NDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 0573-0180-21 | Haleon US Holdings LLC | NDA019771 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 71205-425-24 | Proficient Rx LP | NDA020944 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 50580-184-01 | Johnson & Johnson Consumer Inc. | NDA020516 | HUMAN OTC DRUG | NDA |
-