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Nytol
Nytol - 10158-043-02 - (diphenhydramine HCl)
Drug Information of Nytol
| Product NDC: | 10158-043 |
| Proprietary Name: | Nytol |
| 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) |
Labeler Information of Nytol
| Product NDC: | 10158-043 |
| Labeler Name: | GlaxoSmithKline consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part338 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110812 |
Package Information of Nytol
| Package NDC: | 10158-043-02 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (10158-043-02) > 8 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Nytol
| NDC Code | 10158-043-02 |
| Proprietary Name | Nytol |
| Package Description | 2 BLISTER PACK in 1 CARTON (10158-043-02) > 8 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 10158-043 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diphenhydramine HCl |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110812 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | GlaxoSmithKline consumer Healthcare LP |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
