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IBUPROFEN
IBUPROFEN - 0363-0003-40 - (ibuprofen)
Drug Information of IBUPROFEN
| Product NDC: | 0363-0003 |
| Proprietary Name: | IBUPROFEN |
| Non Proprietary Name: | ibuprofen |
| Active Ingredient(s): | 200 mg/1 & nbsp; ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IBUPROFEN
| Product NDC: | 0363-0003 |
| Labeler Name: | Walgreen Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079205 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110509 |
Package Information of IBUPROFEN
| Package NDC: | 0363-0003-40 |
| Package Description: | 1 BOTTLE in 1 CARTON (0363-0003-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE |
NDC Information of IBUPROFEN
| NDC Code | 0363-0003-40 |
| Proprietary Name | IBUPROFEN |
| Package Description | 1 BOTTLE in 1 CARTON (0363-0003-40) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE |
| Product NDC | 0363-0003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ibuprofen |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20110509 |
| Marketing Category Name | ANDA |
| Labeler Name | Walgreen Company |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
