Cholestyramine
- Product NDC
- 72162-1505
- 11-digit product format
- 721621505
- Labeler code
- 72162
- Product ID
- 72162-1505_fa6509db-b5e2-4210-873b-f0ff4ddc010a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cholestyramine
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077203
- Marketing category
- ANDA
- Marketing start
- 2005-09-15
- Substance
- CHOLESTYRAMINE
- Active strength
- 4 g/5g
- Pharmacologic classes
- Bile Acid Sequestrant [EPC], Bile-acid Binding Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cholestyramine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CHOLESTYRAMINE | 4 g/5g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4B33BGI082 |
| Rxcui | 1801279 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1505-2 | Cholestyramine | 210 g in 1 CAN | POWDER, FOR SUSPENSION | 210 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1505 | CHOLESTYRAMINE POWDER, FOR SUSPENSION [BRYANT RANCH PREPACK] | 101 | Current NDC, 1 package rows | 20240824_c58d6bd9-0273-4c16-8533-495170413d8c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1505-2 | 72162150502 | 210 g in 1 CAN (72162-1505-2) | 210 g | 2024-03-15 | No | No | Historical |