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leader ibuprofen pm
leader ibuprofen pm - 37205-672-60 - (Diphenhydramine citrate, Ibuprofen)
Drug Information of leader ibuprofen pm
| Product NDC: | 37205-672 |
| Proprietary Name: | leader 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 leader ibuprofen pm
| Product NDC: | 37205-672 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079113 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120613 |
Package Information of leader ibuprofen pm
| Package NDC: | 37205-672-60 |
| Package Description: | 1 BOTTLE in 1 CARTON (37205-672-60) > 20 TABLET, COATED in 1 BOTTLE |
NDC Information of leader ibuprofen pm
| NDC Code | 37205-672-60 |
| Proprietary Name | leader ibuprofen pm |
| Package Description | 1 BOTTLE in 1 CARTON (37205-672-60) > 20 TABLET, COATED in 1 BOTTLE |
| Product NDC | 37205-672 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine citrate, Ibuprofen |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120613 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | DIPHENHYDRAMINE CITRATE; IBUPROFEN |
| Strength Number | 38; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
