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HISTAPRIN
HISTAPRIN - 50332-0132-4 - (DIPHENHYDRAMINE)
Drug Information of HISTAPRIN
| Product NDC: | 50332-0132 |
| Proprietary Name: | HISTAPRIN |
| Non Proprietary Name: | DIPHENHYDRAMINE |
| Active Ingredient(s): | 25 mg/1 & nbsp; DIPHENHYDRAMINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HISTAPRIN
| Product NDC: | 50332-0132 |
| Labeler Name: | NorMed |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090101 |
Package Information of HISTAPRIN
| Package NDC: | 50332-0132-4 |
| Package Description: | 50 TABLET in 1 BOX, UNIT-DOSE (50332-0132-4) |
NDC Information of HISTAPRIN
| NDC Code | 50332-0132-4 |
| Proprietary Name | HISTAPRIN |
| Package Description | 50 TABLET in 1 BOX, UNIT-DOSE (50332-0132-4) |
| Product NDC | 50332-0132 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | NorMed |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
