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Fosinopril sodium
Fosinopril sodium - 76282-202-90 - (Fosinopril sodium)
Drug Information of Fosinopril sodium
| Product NDC: | 76282-202 |
| Proprietary Name: | Fosinopril sodium |
| Non Proprietary Name: | Fosinopril sodium |
| Active Ingredient(s): | 40 mg/1 & nbsp; Fosinopril sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fosinopril sodium
| Product NDC: | 76282-202 |
| Labeler Name: | Exelan Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077222 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050621 |
Package Information of Fosinopril sodium
| Package NDC: | 76282-202-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (76282-202-90) |
NDC Information of Fosinopril sodium
| NDC Code | 76282-202-90 |
| Proprietary Name | Fosinopril sodium |
| Package Description | 90 TABLET in 1 BOTTLE (76282-202-90) |
| Product NDC | 76282-202 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fosinopril sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050621 |
| Marketing Category Name | ANDA |
| Labeler Name | Exelan Pharmaceuticals, Inc. |
| Substance Name | FOSINOPRIL SODIUM |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
