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sunmark ibuprofen
sunmark ibuprofen - 49348-374-69 - (ibuprofen)
Drug Information of sunmark ibuprofen
| Product NDC: | 49348-374 |
| Proprietary Name: | sunmark ibuprofen |
| Non Proprietary Name: | ibuprofen |
| Active Ingredient(s): | 50 mg/1.25mL & nbsp; ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sunmark ibuprofen
| Product NDC: | 49348-374 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075217 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030828 |
Package Information of sunmark ibuprofen
| Package NDC: | 49348-374-69 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-374-69) > 15 mL in 1 BOTTLE |
NDC Information of sunmark ibuprofen
| NDC Code | 49348-374-69 |
| Proprietary Name | sunmark ibuprofen |
| Package Description | 1 BOTTLE in 1 CARTON (49348-374-69) > 15 mL in 1 BOTTLE |
| Product NDC | 49348-374 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ibuprofen |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20030828 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | IBUPROFEN |
| Strength Number | 50 |
| Strength Unit | mg/1.25mL |
| Pharmaceutical Classes |
