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Ibuprofen
Ibuprofen - 50844-291-03 - (ibuprofen)
Drug Information of Ibuprofen
| Product NDC: | 50844-291 |
| Proprietary Name: | Ibuprofen |
| Non Proprietary Name: | ibuprofen |
| Active Ingredient(s): | 200 mg/1 & nbsp; ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ibuprofen
| Product NDC: | 50844-291 |
| Labeler Name: | L.N.K. International, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075010 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990302 |
Package Information of Ibuprofen
| Package NDC: | 50844-291-03 |
| Package Description: | 10 TABLET, FILM COATED in 1 VIAL, PLASTIC (50844-291-03) |
NDC Information of Ibuprofen
| NDC Code | 50844-291-03 |
| Proprietary Name | Ibuprofen |
| Package Description | 10 TABLET, FILM COATED in 1 VIAL, PLASTIC (50844-291-03) |
| Product NDC | 50844-291 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ibuprofen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19990302 |
| Marketing Category Name | ANDA |
| Labeler Name | L.N.K. International, Inc. |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
