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Captopril
Captopril - 68645-162-59 - (Captopril)
Drug Information of Captopril
| Product NDC: | 68645-162 |
| Proprietary Name: | Captopril |
| Non Proprietary Name: | Captopril |
| Active Ingredient(s): | 50 mg/1 & nbsp; Captopril |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Captopril
| Product NDC: | 68645-162 |
| Labeler Name: | Legacy Pharmaceutical Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074532 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090911 |
Package Information of Captopril
| Package NDC: | 68645-162-59 |
| Package Description: | 60 TABLET in 1 BOTTLE (68645-162-59) |
NDC Information of Captopril
| NDC Code | 68645-162-59 |
| Proprietary Name | Captopril |
| Package Description | 60 TABLET in 1 BOTTLE (68645-162-59) |
| Product NDC | 68645-162 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Captopril |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090911 |
| Marketing Category Name | ANDA |
| Labeler Name | Legacy Pharmaceutical Packaging |
| Substance Name | CAPTOPRIL |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
