Product NDC: | 76270-109 |
Proprietary Name: | NIGHTTIME SLEEP AID |
Non Proprietary Name: | DIPHENHYDRAMINE HYDROCHLORIDE 50 mg |
Active Ingredient(s): | 50 mg/1 & nbsp; DIPHENHYDRAMINE HYDROCHLORIDE 50 mg |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76270-109 |
Labeler Name: | PuraVation Pharmaceuticals Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130415 |
Package NDC: | 76270-109-17 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (76270-109-17) > 64 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC |
NDC Code | 76270-109-17 |
Proprietary Name | NIGHTTIME SLEEP AID |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (76270-109-17) > 64 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC |
Product NDC | 76270-109 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE 50 mg |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20130415 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | PuraVation Pharmaceuticals Inc |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes |