cholestyramine light is a Oral Powder, For Suspension in the Human Prescription Drug category. It is labeled and distributed by Eon Labs, Inc.. The primary component is Cholestyramine.
| Product ID | 0185-0939_0ec9ae89-efd0-4c8f-88e0-944d72eda831 |
| NDC | 0185-0939 |
| Product Type | Human Prescription Drug |
| Proprietary Name | cholestyramine light |
| Generic Name | Cholestyramine Light |
| Dosage Form | Powder, For Suspension |
| Route of Administration | ORAL |
| Marketing Start Date | 1994-11-04 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA074558 |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | CHOLESTYRAMINE |
| Active Ingredient Strength | 4 g/5.7g |
| Pharm Classes | Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 1994-11-04 |
| Marketing End Date | 2025-07-31 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA074558 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1994-11-04 |
| Marketing Category | ANDA |
| Application Number | ANDA074558 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 1994-11-04 |
| Ingredient | Strength |
|---|---|
| CHOLESTYRAMINE | 4 g/5.7g |
| SPL SET ID: | a7dd335a-6413-446e-8098-d4f97e935986 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0185-0939 | cholestyramine light | cholestyramine light |
| 42806-269 | CHOLESTYRAMINE LIGHT | cholestyramine light |
| 42806-270 | CHOLESTYRAMINE LIGHT | cholestyramine light |
| 42806-271 | CHOLESTYRAMINE LIGHT | cholestyramine light |
| 51224-009 | Cholestyramine Light | Cholestyramine |
| 56156-001 | Cholestyramine Light | Cholestyramine |