cholestyramine powder for suspension
- Product NDC
- 71335-2902
- 11-digit product format
- 713352902
- Labeler code
- 71335
- Product ID
- 71335-2902_2800a72a-4af8-461b-952f-8237b2d6e535
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cholestyramine powder for suspension
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211856
- Marketing category
- ANDA
- Marketing start
- 2021-10-20
- Substance
- CHOLESTYRAMINE
- Active strength
- 4 g/8.78g
- Pharmacologic classes
- Bile Acid Sequestrant [EPC], Bile-acid Binding Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- cholestyramine powder for suspension
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CHOLESTYRAMINE | 4 g/8.78g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4B33BGI082 |
| Rxcui | 848943 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2902-1 | cholestyramine powder for suspension | 368.760 g in 1 CAN | POWDER, FOR SUSPENSION | 368.760 | | 101 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2902-1 | 71335290201 | 368.76 g in 1 CAN (71335-2902-1) | 368.76 g | 2025-11-07 | No | No | Current |