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SnoozEase
SnoozEase - 59726-225-12 - (Diphenhydramine Hydrochloride)
Drug Information of SnoozEase
| Product NDC: | 59726-225 |
| Proprietary Name: | SnoozEase |
| Non Proprietary Name: | Diphenhydramine Hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SnoozEase
| Product NDC: | 59726-225 |
| Labeler Name: | P and L Development of New York Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part338 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130411 |
Package Information of SnoozEase
| Package NDC: | 59726-225-12 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59726-225-12) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of SnoozEase
| NDC Code | 59726-225-12 |
| Proprietary Name | SnoozEase |
| Package Description | 1 BLISTER PACK in 1 CARTON (59726-225-12) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 59726-225 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20130411 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | P and L Development of New York Corporation |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
