Home
>
National Drug Code (NDC)
>
up and up dye free infants concentrated ibuprofen
up and up dye free infants concentrated ibuprofen - 11673-255-10 - (Ibuprofen)
Drug Information of up and up dye free infants concentrated ibuprofen
| Product NDC: | 11673-255 |
| Proprietary Name: | up and up dye free infants concentrated ibuprofen |
| Non Proprietary Name: | Ibuprofen |
| Active Ingredient(s): | 50 mg/1.25mL & nbsp; Ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of up and up dye free infants concentrated ibuprofen
| Product NDC: | 11673-255 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075217 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090708 |
Package Information of up and up dye free infants concentrated ibuprofen
| Package NDC: | 11673-255-10 |
| Package Description: | 1 BOTTLE in 1 CARTON (11673-255-10) > 30 mL in 1 BOTTLE |
NDC Information of up and up dye free infants concentrated ibuprofen
| NDC Code | 11673-255-10 |
| Proprietary Name | up and up dye free infants concentrated ibuprofen |
| Package Description | 1 BOTTLE in 1 CARTON (11673-255-10) > 30 mL in 1 BOTTLE |
| Product NDC | 11673-255 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | SUSPENSION/ DROPS |
| Route Name | ORAL |
| Start Marketing Date | 20090708 |
| Marketing Category Name | ANDA |
| Labeler Name | Target Corporation |
| Substance Name | IBUPROFEN |
| Strength Number | 50 |
| Strength Unit | mg/1.25mL |
| Pharmaceutical Classes |
