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BENAZEPRIL HYDROCHLORIDE
BENAZEPRIL HYDROCHLORIDE - 13811-628-10 - (Benazepril hydrochloride)
Drug Information of BENAZEPRIL HYDROCHLORIDE
| Product NDC: | 13811-628 |
| Proprietary Name: | BENAZEPRIL HYDROCHLORIDE |
| Non Proprietary Name: | Benazepril hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Benazepril hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BENAZEPRIL HYDROCHLORIDE
| Product NDC: | 13811-628 |
| Labeler Name: | Trigen Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076118 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121115 |
Package Information of BENAZEPRIL HYDROCHLORIDE
| Package NDC: | 13811-628-10 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (13811-628-10) |
NDC Information of BENAZEPRIL HYDROCHLORIDE
| NDC Code | 13811-628-10 |
| Proprietary Name | BENAZEPRIL HYDROCHLORIDE |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (13811-628-10) |
| Product NDC | 13811-628 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Benazepril hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121115 |
| Marketing Category Name | ANDA |
| Labeler Name | Trigen Laboratories, Inc. |
| Substance Name | BENAZEPRIL HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
