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CHILDRENS ADVIL
CHILDRENS ADVIL - 0573-0170-30 - (IBUPROFEN)
Drug Information of CHILDRENS ADVIL
| Product NDC: | 0573-0170 |
| Proprietary Name: | CHILDRENS ADVIL |
| Non Proprietary Name: | IBUPROFEN |
| Active Ingredient(s): | 100 mg/5mL & nbsp; IBUPROFEN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CHILDRENS ADVIL
| Product NDC: | 0573-0170 |
| Labeler Name: | Pfizer Consumer Healthcare |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020589 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960627 |
Package Information of CHILDRENS ADVIL
| Package NDC: | 0573-0170-30 |
| Package Description: | 1 BOTTLE in 1 CARTON (0573-0170-30) > 120 mL in 1 BOTTLE |
NDC Information of CHILDRENS ADVIL
| NDC Code | 0573-0170-30 |
| Proprietary Name | CHILDRENS ADVIL |
| Package Description | 1 BOTTLE in 1 CARTON (0573-0170-30) > 120 mL in 1 BOTTLE |
| Product NDC | 0573-0170 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | IBUPROFEN |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 19960627 |
| Marketing Category Name | NDA |
| Labeler Name | Pfizer Consumer Healthcare |
| Substance Name | IBUPROFEN |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
