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Diphenhydramine HCl
Diphenhydramine HCl - 62211-048-99 - (Diphenhydramine HCl)
Drug Information of Diphenhydramine HCl
| Product NDC: | 62211-048 |
| 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, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diphenhydramine HCl
| Product NDC: | 62211-048 |
| Labeler Name: | A&Z Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20030310 |
Package Information of Diphenhydramine HCl
| Package NDC: | 62211-048-99 |
| Package Description: | 69767 TABLET, COATED in 1 CARTON (62211-048-99) |
NDC Information of Diphenhydramine HCl
| NDC Code | 62211-048-99 |
| Proprietary Name | Diphenhydramine HCl |
| Package Description | 69767 TABLET, COATED in 1 CARTON (62211-048-99) |
| Product NDC | 62211-048 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine HCl |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20030310 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | A&Z Pharmaceutical, Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
