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Ibutab
Ibutab - 35418-750-69 - (Ibuprofen)
Drug Information of Ibutab
| Product NDC: | 35418-750 |
| Proprietary Name: | Ibutab |
| 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 Ibutab
| Product NDC: | 35418-750 |
| Labeler Name: | Zee Medical Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079129 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120612 |
Package Information of Ibutab
| Package NDC: | 35418-750-69 |
| Package Description: | 500 CARTON in 1 CARTON (35418-750-69) > 125 CARTON in 1 CARTON (35418-750-67) > 50 PACKET in 1 CARTON (35418-750-68) > 2 TABLET in 1 PACKET (35418-750-02) |
NDC Information of Ibutab
| NDC Code | 35418-750-69 |
| Proprietary Name | Ibutab |
| Package Description | 500 CARTON in 1 CARTON (35418-750-69) > 125 CARTON in 1 CARTON (35418-750-67) > 50 PACKET in 1 CARTON (35418-750-68) > 2 TABLET in 1 PACKET (35418-750-02) |
| Product NDC | 35418-750 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120612 |
| Marketing Category Name | ANDA |
| Labeler Name | Zee Medical Inc |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
