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Banophen
Banophen - 0904-5174-16 - (diphenhydramine hydrochloride)
Drug Information of Banophen
| Product NDC: | 0904-5174 |
| Proprietary Name: | Banophen |
| Non Proprietary Name: | diphenhydramine hydrochloride |
| Active Ingredient(s): | 12.5 mg/5mL & nbsp; diphenhydramine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Banophen
| Product NDC: | 0904-5174 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120824 |
Package Information of Banophen
| Package NDC: | 0904-5174-16 |
| Package Description: | 473 mL in 1 BOTTLE (0904-5174-16) |
NDC Information of Banophen
| NDC Code | 0904-5174-16 |
| Proprietary Name | Banophen |
| Package Description | 473 mL in 1 BOTTLE (0904-5174-16) |
| Product NDC | 0904-5174 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diphenhydramine hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120824 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 12.5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
