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 |
---|---|---|---|---|---|
PRASTERONE; IBUPROFEN | 55607-400-10 | Health Science Funding, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
IBUPROFEN | 69517-111-02 | HealthLife of USA LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 69517-111-25 | HealthLife of USA LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 69517-111-30 | HealthLife of USA LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 69517-111-05 | HealthLife of USA LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 69517-111-50 | HealthLife of USA LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 69517-111-10 | HealthLife of USA LLC | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-109-08 | HEB | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-109-10 | HEB | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-109-03 | HEB | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-609-11 | HEB | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-410-05 | HEB | ANDA079174 | HUMAN OTC DRUG | ANDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 37808-324-40 | HEB | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-609-83 | HEB | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-410-02 | HEB | ANDA079174 | HUMAN OTC DRUG | ANDA |
PSEUDOEPHEDRINE HYDROCHLORIDE; IBUPROFEN | 37808-423-40 | HEB | ANDA074567 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 37808-609-78 | HEB | ANDA078682 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 49260-615-50 | Help Remedies, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 49260-615-16 | Help Remedies, Inc. | ANDA075139 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0404-0017-99 | Henry Schein Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 0404-0017-13 | Henry Schein Inc. | ANDA075010 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; ACETAMINOPHEN | 0143-9150-10 | Hikma Pharmaceuticals USA Inc. | NDA215320 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN; ACETAMINOPHEN | 0143-9150-01 | Hikma Pharmaceuticals USA Inc. | NDA215320 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN; FAMOTIDINE | 75987-010-72 | Horizon Therapeutics USA, Inc. | NDA022519 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN; FAMOTIDINE | 75987-010-03 | Horizon Therapeutics USA, Inc. | NDA022519 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN | 53345-014-01 | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 53345-050-01 | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 53345-039-03 | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 53345-039-01 | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd | ANDA206568 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 53345-014-02 | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd | ANDA206568 | HUMAN OTC DRUG | ANDA |
-