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lisinopril
lisinopril - 0185-0101-10 - (lisinopril)
Drug Information of lisinopril
| Product NDC: | 0185-0101 |
| Proprietary Name: | lisinopril |
| Non Proprietary Name: | lisinopril |
| Active Ingredient(s): | 10 mg/1 & nbsp; lisinopril |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of lisinopril
| Product NDC: | 0185-0101 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075994 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020701 |
Package Information of lisinopril
| Package NDC: | 0185-0101-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (0185-0101-10) |
NDC Information of lisinopril
| NDC Code | 0185-0101-10 |
| Proprietary Name | lisinopril |
| Package Description | 1000 TABLET in 1 BOTTLE (0185-0101-10) |
| Product NDC | 0185-0101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lisinopril |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20020701 |
| Marketing Category Name | ANDA |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | LISINOPRIL |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
