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Sominex
Sominex - 0135-0057-16 - (diphenhydramine HCl)
Drug Information of Sominex
| Product NDC: | 0135-0057 |
| Proprietary Name: | Sominex |
| Non Proprietary Name: | diphenhydramine HCl |
| Active Ingredient(s): | 25 mg/1 & nbsp; diphenhydramine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sominex
| Product NDC: | 0135-0057 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part338 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101108 |
Package Information of Sominex
| Package NDC: | 0135-0057-16 |
| Package Description: | 72 TABLET in 1 BLISTER PACK (0135-0057-16) |
NDC Information of Sominex
| NDC Code | 0135-0057-16 |
| Proprietary Name | Sominex |
| Package Description | 72 TABLET in 1 BLISTER PACK (0135-0057-16) |
| Product NDC | 0135-0057 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diphenhydramine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101108 |
| 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 |
