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ZzzQuil
ZzzQuil - 37000-501-12 - (Diphenhydramine Hydrochloride)
Drug Information of ZzzQuil
| Product NDC: | 37000-501 |
| Proprietary Name: | ZzzQuil |
| Non Proprietary Name: | Diphenhydramine Hydrochloride |
| Active Ingredient(s): | 50 mg/21 & nbsp; Diphenhydramine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, GELATIN COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZzzQuil
| Product NDC: | 37000-501 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part338 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111208 |
Package Information of ZzzQuil
| Package NDC: | 37000-501-12 |
| Package Description: | 6 BLISTER PACK in 1 CARTON (37000-501-12) > 2 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
NDC Information of ZzzQuil
| NDC Code | 37000-501-12 |
| Proprietary Name | ZzzQuil |
| Package Description | 6 BLISTER PACK in 1 CARTON (37000-501-12) > 2 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
| Product NDC | 37000-501 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | CAPSULE, GELATIN COATED |
| Route Name | ORAL |
| Start Marketing Date | 20111208 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/21 |
| Pharmaceutical Classes |
