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 | 67751-120-01 | Navajo Manufacturing Company Inc. | NDA019012 | HUMAN OTC DRUG | NDA |
PHENYLEPHRINE HYDROCHLORIDE; IBUPROFEN | 67751-150-01 | Navajo Manufacturing Company Inc. | NDA022565 | HUMAN OTC DRUG | NDA |
CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE | 67751-149-01 | Navajo Manufacturing Company Inc. | NDA022113 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 67751-147-01 | Navajo Manufacturing Company Inc. | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-148-01 | Navajo Manufacturing Company Inc. | NDA020402 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; IBUPROFEN | 67751-211-02 | Navajo Manufacturing Company Inc. | NDA211733 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 67751-146-03 | Navajo Manufacturing Company Inc. | NDA018989 | HUMAN OTC DRUG | NDA |
ACETAMINOPHEN; IBUPROFEN | 67751-211-01 | Navajo Manufacturing Company Inc. | NDA211733 | HUMAN OTC DRUG | NDA |
DIPHENHYDRAMINE CITRATE; IBUPROFEN | 67751-147-02 | Navajo Manufacturing Company Inc. | NDA021394 | HUMAN OTC DRUG | NDA |
IBUPROFEN | 0615-8309-39 | NCS HealthCare of KY, Inc dba Vangard Labs | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 0615-8311-39 | NCS HealthCare of KY, Inc dba Vangard Labs | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 0615-8310-39 | NCS HealthCare of KY, Inc dba Vangard Labs | ANDA078329 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51824-064-01 | New World Imports | ANDA079174 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 50332-0109-7 | NorMed | part343 | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN | 50332-0109-4 | NorMed | part343 | HUMAN OTC DRUG | OTC monograph not final |
IBUPROFEN | 51655-757-26 | Northwind Pharmaceuticals | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51655-474-52 | Northwind Pharmaceuticals | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-385-51 | Northwind Pharmaceuticals | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-051-25 | Northwind Pharmaceuticals | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-048-52 | Northwind Pharmaceuticals | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-275-21 | Northwind Pharmaceuticals | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-385-25 | Northwind Pharmaceuticals | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-385-52 | Northwind Pharmaceuticals | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-275-20 | Northwind Pharmaceuticals | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-385-54 | Northwind Pharmaceuticals | ANDA091625 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-275-26 | Northwind Pharmaceuticals | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-757-52 | Northwind Pharmaceuticals | ANDA072096 | HUMAN OTC DRUG | ANDA |
IBUPROFEN | 51655-275-54 | Northwind Pharmaceuticals | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-474-26 | Northwind Pharmaceuticals | ANDA090796 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN | 51655-051-54 | Northwind Pharmaceuticals | ANDA078558 | HUMAN PRESCRIPTION DRUG | ANDA |
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