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Ibuprofen PM
Ibuprofen PM - 0363-0050-48 - (diphenhydramine citrate, ibuprofen)
Drug Information of Ibuprofen PM
| Product NDC: | 0363-0050 |
| Proprietary Name: | Ibuprofen PM |
| Non Proprietary Name: | diphenhydramine citrate, ibuprofen |
| Active Ingredient(s): | 38; 200 mg/1; mg/1 & nbsp; diphenhydramine citrate, ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ibuprofen PM
| Product NDC: | 0363-0050 |
| Labeler Name: | Walgreen Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079113 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090219 |
Package Information of Ibuprofen PM
| Package NDC: | 0363-0050-48 |
| Package Description: | 1 BOTTLE in 1 CARTON (0363-0050-48) > 180 TABLET, COATED in 1 BOTTLE |
NDC Information of Ibuprofen PM
| NDC Code | 0363-0050-48 |
| Proprietary Name | Ibuprofen PM |
| Package Description | 1 BOTTLE in 1 CARTON (0363-0050-48) > 180 TABLET, COATED in 1 BOTTLE |
| Product NDC | 0363-0050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diphenhydramine citrate, ibuprofen |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090219 |
| Marketing Category Name | ANDA |
| Labeler Name | Walgreen Company |
| Substance Name | DIPHENHYDRAMINE CITRATE; IBUPROFEN |
| Strength Number | 38; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
