| Product NDC: | 59779-367 |
| Proprietary Name: | Nighttime Sleep Aid |
| Non Proprietary Name: | Diphenhydramine HCl |
| Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59779-367 |
| Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part338 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20000610 |
| Package NDC: | 59779-367-22 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59779-367-22) > 48 TABLET, FILM COATED in 1 BLISTER PACK |
| NDC Code | 59779-367-22 |
| Proprietary Name | Nighttime Sleep Aid |
| Package Description | 1 BLISTER PACK in 1 CARTON (59779-367-22) > 48 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 59779-367 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine HCl |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20000610 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |