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Advil
Advil - 0573-0133-02 - (ibuprofen sodium)
Drug Information of Advil
| Product NDC: | 0573-0133 |
| Proprietary Name: | Advil |
| Non Proprietary Name: | ibuprofen sodium |
| Active Ingredient(s): | 256 mg/1 & nbsp; ibuprofen sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Advil
| Product NDC: | 0573-0133 |
| Labeler Name: | Pfizer Consumer Healthcare |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA201803 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130708 |
Package Information of Advil
| Package NDC: | 0573-0133-02 |
| Package Description: | 50 PACKET in 1 TRAY (0573-0133-02) > 2 TABLET, COATED in 1 PACKET |
NDC Information of Advil
| NDC Code | 0573-0133-02 |
| Proprietary Name | Advil |
| Package Description | 50 PACKET in 1 TRAY (0573-0133-02) > 2 TABLET, COATED in 1 PACKET |
| Product NDC | 0573-0133 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ibuprofen sodium |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130708 |
| Marketing Category Name | NDA |
| Labeler Name | Pfizer Consumer Healthcare |
| Substance Name | IBUPROFEN SODIUM |
| Strength Number | 256 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
