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Advil PM
Advil PM - 66715-9733-8 - (Ibuprofen and Diphenhydramine citrate)
Drug Information of Advil PM
| Product NDC: | 66715-9733 |
| Proprietary Name: | Advil PM |
| Non Proprietary Name: | Ibuprofen and Diphenhydramine citrate |
| Active Ingredient(s): | 38; 200 mg/1; mg/1 & nbsp; Ibuprofen and Diphenhydramine citrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Advil PM
| Product NDC: | 66715-9733 |
| Labeler Name: | Lil' Drug Store Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021394 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100511 |
Package Information of Advil PM
| Package NDC: | 66715-9733-8 |
| Package Description: | 5 POUCH in 1 CARTON (66715-9733-8) > 2 TABLET, COATED in 1 POUCH |
NDC Information of Advil PM
| NDC Code | 66715-9733-8 |
| Proprietary Name | Advil PM |
| Package Description | 5 POUCH in 1 CARTON (66715-9733-8) > 2 TABLET, COATED in 1 POUCH |
| Product NDC | 66715-9733 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen and Diphenhydramine citrate |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100511 |
| Marketing Category Name | NDA |
| Labeler Name | Lil' Drug Store Products, Inc. |
| Substance Name | DIPHENHYDRAMINE CITRATE; IBUPROFEN |
| Strength Number | 38; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
