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PROBUFEN
PROBUFEN - 49789-050-01 - (IBUPROFEN)
Drug Information of PROBUFEN
| Product NDC: | 49789-050 |
| Proprietary Name: | PROBUFEN |
| Non Proprietary Name: | IBUPROFEN |
| Active Ingredient(s): | 400 mg/537mg & nbsp; IBUPROFEN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PROBUFEN
| Product NDC: | 49789-050 |
| Labeler Name: | SAMSUNG PHARM IND. CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111201 |
Package Information of PROBUFEN
| Package NDC: | 49789-050-01 |
| Package Description: | 537 mg in 1 BLISTER PACK (49789-050-01) |
NDC Information of PROBUFEN
| NDC Code | 49789-050-01 |
| Proprietary Name | PROBUFEN |
| Package Description | 537 mg in 1 BLISTER PACK (49789-050-01) |
| Product NDC | 49789-050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | IBUPROFEN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SAMSUNG PHARM IND. CO., LTD. |
| Substance Name | IBUPROFEN |
| Strength Number | 400 |
| Strength Unit | mg/537mg |
| Pharmaceutical Classes |
