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Advil
Advil - 66715-9700-3 - (Ibuprofen)
Drug Information of Advil
| Product NDC: | 66715-9700 |
| Proprietary Name: | Advil |
| Non Proprietary Name: | Ibuprofen |
| Active Ingredient(s): | 200 mg/1 & nbsp; Ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Advil
| Product NDC: | 66715-9700 |
| Labeler Name: | Lil' Drug Store Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA018989 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100222 |
Package Information of Advil
| Package NDC: | 66715-9700-3 |
| Package Description: | 3 POUCH in 1 CARTON (66715-9700-3) > 2 TABLET, COATED in 1 POUCH |
NDC Information of Advil
| NDC Code | 66715-9700-3 |
| Proprietary Name | Advil |
| Package Description | 3 POUCH in 1 CARTON (66715-9700-3) > 2 TABLET, COATED in 1 POUCH |
| Product NDC | 66715-9700 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100222 |
| Marketing Category Name | NDA |
| Labeler Name | Lil' Drug Store Products, Inc. |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
