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IBUPROFEN
IBUPROFEN - 12634-860-01 - (IBUPROFEN)
Drug Information of IBUPROFEN
| Product NDC: | 12634-860 |
| Proprietary Name: | IBUPROFEN |
| Non Proprietary Name: | IBUPROFEN |
| Active Ingredient(s): | 200 mg/1 & nbsp; IBUPROFEN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IBUPROFEN
| Product NDC: | 12634-860 |
| Labeler Name: | Apotheca Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA071333 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090916 |
Package Information of IBUPROFEN
| Package NDC: | 12634-860-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (12634-860-01) |
NDC Information of IBUPROFEN
| NDC Code | 12634-860-01 |
| Proprietary Name | IBUPROFEN |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (12634-860-01) |
| Product NDC | 12634-860 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | IBUPROFEN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090916 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotheca Inc. |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
