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diphenhydramine hydrochloride
diphenhydramine hydrochloride - 0185-0649-01 - (diphenhydramine hydrochloride)
Drug Information of diphenhydramine hydrochloride
| Product NDC: | 0185-0649 |
| Proprietary Name: | diphenhydramine hydrochloride |
| Non Proprietary Name: | diphenhydramine hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; diphenhydramine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of diphenhydramine hydrochloride
| Product NDC: | 0185-0649 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20000501 |
Package Information of diphenhydramine hydrochloride
| Package NDC: | 0185-0649-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (0185-0649-01) |
NDC Information of diphenhydramine hydrochloride
| NDC Code | 0185-0649-01 |
| Proprietary Name | diphenhydramine hydrochloride |
| Package Description | 100 CAPSULE in 1 BOTTLE (0185-0649-01) |
| Product NDC | 0185-0649 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diphenhydramine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20000501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
