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Diphenhydramine
Diphenhydramine - 57344-090-01 - (DIPHENHYDRAMINE HYDROCHLORIDE)
Drug Information of Diphenhydramine
| Product NDC: | 57344-090 |
| Proprietary Name: | Diphenhydramine |
| Non Proprietary Name: | DIPHENHYDRAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 25 mg/1 & nbsp; DIPHENHYDRAMINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diphenhydramine
| Product NDC: | 57344-090 |
| Labeler Name: | AAA Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121222 |
Package Information of Diphenhydramine
| Package NDC: | 57344-090-01 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (57344-090-01) > 12 TABLET, COATED in 1 BLISTER PACK |
NDC Information of Diphenhydramine
| NDC Code | 57344-090-01 |
| Proprietary Name | Diphenhydramine |
| Package Description | 2 BLISTER PACK in 1 CARTON (57344-090-01) > 12 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 57344-090 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121222 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | AAA Pharmaceutical, Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
