| Product NDC: | 76457-002 |
| Proprietary Name: | diphenhydramine hydrochloride |
| Non Proprietary Name: | DIPHENHYDRAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 25 mg/1 & nbsp; DIPHENHYDRAMINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76457-002 |
| Labeler Name: | Simpex Pharma Pvt. Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121115 |
| Package NDC: | 76457-002-00 |
| Package Description: | 1 BOTTLE in 1 CARTON (76457-002-00) > 100 TABLET in 1 BOTTLE |
| NDC Code | 76457-002-00 |
| Proprietary Name | diphenhydramine hydrochloride |
| Package Description | 1 BOTTLE in 1 CARTON (76457-002-00) > 100 TABLET in 1 BOTTLE |
| Product NDC | 76457-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121115 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Simpex Pharma Pvt. Ltd |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |