Home
>
National Drug Code (NDC)
>
LISINOPRIL
LISINOPRIL - 10544-239-30 - (LISINOPRIL)
Drug Information of LISINOPRIL
| Product NDC: | 10544-239 |
| Proprietary Name: | LISINOPRIL |
| Non Proprietary Name: | LISINOPRIL |
| Active Ingredient(s): | 20 mg/1 & nbsp; LISINOPRIL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LISINOPRIL
| Product NDC: | 10544-239 |
| Labeler Name: | Blenheim Pharmacal, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077321 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091216 |
Package Information of LISINOPRIL
| Package NDC: | 10544-239-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (10544-239-30) |
NDC Information of LISINOPRIL
| NDC Code | 10544-239-30 |
| Proprietary Name | LISINOPRIL |
| Package Description | 30 TABLET in 1 BOTTLE (10544-239-30) |
| Product NDC | 10544-239 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LISINOPRIL |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091216 |
| Marketing Category Name | ANDA |
| Labeler Name | Blenheim Pharmacal, Inc. |
| Substance Name | LISINOPRIL |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
