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Banophen
Banophen - 0904-2035-59 - (Diphenhydramine HCl)
Drug Information of Banophen
| Product NDC: | 0904-2035 |
| Proprietary Name: | Banophen |
| Non Proprietary Name: | Diphenhydramine HCl |
| Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Banophen
| Product NDC: | 0904-2035 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19900315 |
Package Information of Banophen
| Package NDC: | 0904-2035-59 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0904-2035-59) > 100 CAPSULE in 1 BOTTLE, PLASTIC |
NDC Information of Banophen
| NDC Code | 0904-2035-59 |
| Proprietary Name | Banophen |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0904-2035-59) > 100 CAPSULE in 1 BOTTLE, PLASTIC |
| Product NDC | 0904-2035 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine HCl |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19900315 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
