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Concentrated Ibuprofen
Concentrated Ibuprofen - 27808-007-02 - (Concentrated Ibuprofen)
Drug Information of Concentrated Ibuprofen
| Product NDC: | 27808-007 |
| Proprietary Name: | Concentrated Ibuprofen |
| Non Proprietary Name: | Concentrated Ibuprofen |
| Active Ingredient(s): | 50 mg/1.25mL & nbsp; Concentrated Ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Concentrated Ibuprofen
| Product NDC: | 27808-007 |
| Labeler Name: | Tris Phrama Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079058 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121106 |
Package Information of Concentrated Ibuprofen
| Package NDC: | 27808-007-02 |
| Package Description: | 30 mL in 1 BOTTLE, PLASTIC (27808-007-02) |
NDC Information of Concentrated Ibuprofen
| NDC Code | 27808-007-02 |
| Proprietary Name | Concentrated Ibuprofen |
| Package Description | 30 mL in 1 BOTTLE, PLASTIC (27808-007-02) |
| Product NDC | 27808-007 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Concentrated Ibuprofen |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20121106 |
| Marketing Category Name | ANDA |
| Labeler Name | Tris Phrama Inc |
| Substance Name | IBUPROFEN |
| Strength Number | 50 |
| Strength Unit | mg/1.25mL |
| Pharmaceutical Classes |
