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Nighttime Sleep Aid Maximum Strength
Nighttime Sleep Aid Maximum Strength - 59726-230-32 - (DIPHENHYDRAMINE HYDROCHLORIDE)
Drug Information of Nighttime Sleep Aid Maximum Strength
| Product NDC: | 59726-230 |
| Proprietary Name: | Nighttime Sleep Aid Maximum Strength |
| Non Proprietary Name: | DIPHENHYDRAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 50 mg/1 & nbsp; DIPHENHYDRAMINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nighttime Sleep Aid Maximum Strength
| Product NDC: | 59726-230 |
| 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: | 20110902 |
Package Information of Nighttime Sleep Aid Maximum Strength
| Package NDC: | 59726-230-32 |
| Package Description: | 1 BOTTLE in 1 BOX (59726-230-32) > 32 CAPSULE, LIQUID FILLED in 1 BOTTLE |
NDC Information of Nighttime Sleep Aid Maximum Strength
| NDC Code | 59726-230-32 |
| Proprietary Name | Nighttime Sleep Aid Maximum Strength |
| Package Description | 1 BOTTLE in 1 BOX (59726-230-32) > 32 CAPSULE, LIQUID FILLED in 1 BOTTLE |
| Product NDC | 59726-230 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20110902 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | P and L Development of New York Corporation |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
