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BENALDRYL
BENALDRYL - 42787-104-30 - (DIPHENHYDRAMINE HCL)
Drug Information of BENALDRYL
| Product NDC: | 42787-104 |
| Proprietary Name: | BENALDRYL |
| Non Proprietary Name: | DIPHENHYDRAMINE HCL |
| Active Ingredient(s): | 25 mg/250mg & nbsp; DIPHENHYDRAMINE HCL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BENALDRYL
| Product NDC: | 42787-104 |
| Labeler Name: | AJES PHARMACEUTICALS,LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120901 |
Package Information of BENALDRYL
| Package NDC: | 42787-104-30 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (42787-104-30) > 1250 mg in 1 BOTTLE, PLASTIC |
NDC Information of BENALDRYL
| NDC Code | 42787-104-30 |
| Proprietary Name | BENALDRYL |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (42787-104-30) > 1250 mg in 1 BOTTLE, PLASTIC |
| Product NDC | 42787-104 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE HCL |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | AJES PHARMACEUTICALS,LLC |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/250mg |
| Pharmaceutical Classes |
