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cholestyramine light
cholestyramine light - 0185-0939-97 - (cholestyramine light)
Drug Information of cholestyramine light
| Product NDC: | 0185-0939 |
| Proprietary Name: | cholestyramine light |
| Non Proprietary Name: | cholestyramine light |
| Active Ingredient(s): | 4 g/5.7g & nbsp; cholestyramine light |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of cholestyramine light
| Product NDC: | 0185-0939 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074558 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19941104 |
Package Information of cholestyramine light
| Package NDC: | 0185-0939-97 |
| Package Description: | 239.4 g in 1 CAN (0185-0939-97) |
NDC Information of cholestyramine light
| NDC Code | 0185-0939-97 |
| Proprietary Name | cholestyramine light |
| Package Description | 239.4 g in 1 CAN (0185-0939-97) |
| Product NDC | 0185-0939 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cholestyramine light |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 19941104 |
| Marketing Category Name | ANDA |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | CHOLESTYRAMINE |
| Strength Number | 4 |
| Strength Unit | g/5.7g |
| Pharmaceutical Classes | Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA] |
