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Diphenhydramine HCl
Diphenhydramine HCl - 10267-0835-1 - (Diphenhydramine HCl)
Drug Information of Diphenhydramine HCl
| Product NDC: | 10267-0835 |
| Proprietary Name: | Diphenhydramine HCl |
| 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 Diphenhydramine HCl
| Product NDC: | 10267-0835 |
| Labeler Name: | Contract Pharmacal Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20040101 |
Package Information of Diphenhydramine HCl
| Package NDC: | 10267-0835-1 |
| Package Description: | 100 TABLET in 1 BOTTLE (10267-0835-1) |
NDC Information of Diphenhydramine HCl
| NDC Code | 10267-0835-1 |
| Proprietary Name | Diphenhydramine HCl |
| Package Description | 100 TABLET in 1 BOTTLE (10267-0835-1) |
| Product NDC | 10267-0835 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Contract Pharmacal Corp |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
