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Cholestyramine
Cholestyramine - 49884-466-67 - (cholestyramine)
Drug Information of Cholestyramine
| Product NDC: | 49884-466 |
| Proprietary Name: | Cholestyramine |
| Non Proprietary Name: | cholestyramine |
| Active Ingredient(s): | 4 g/5g & nbsp; cholestyramine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cholestyramine
| Product NDC: | 49884-466 |
| Labeler Name: | Par Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077204 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050915 |
Package Information of Cholestyramine
| Package NDC: | 49884-466-67 |
| Package Description: | 210 g in 1 CAN (49884-466-67) |
NDC Information of Cholestyramine
| NDC Code | 49884-466-67 |
| Proprietary Name | Cholestyramine |
| Package Description | 210 g in 1 CAN (49884-466-67) |
| Product NDC | 49884-466 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cholestyramine |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20050915 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical, Inc. |
| Substance Name | CHOLESTYRAMINE |
| Strength Number | 4 |
| Strength Unit | g/5g |
| Pharmaceutical Classes | Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA] |
