Cholestyramine
- Product NDC
- 42571-508
- 11-digit product format
- 425710508
- Labeler code
- 42571
- Product ID
- 42571-508_4c544fbf-3a7e-d5fa-e063-6394a90a176f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cholestyramine
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Micro Labs Limited
- Application
- ANDA219318
- Marketing category
- ANDA
- Marketing start
- 2026-04-01
- Substance
- CHOLESTYRAMINE
- Active strength
- 4 g/9g
- 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
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CHOLESTYRAMINE | 4 g/9g |
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 |
|---|
| 42571-508-04 | Cholestyramine | 9 g in 1 POUCH | POWDER, FOR SUSPENSION | 9 | | 1 |
| 42571-508-29 | Cholestyramine | 60 in 1 CARTON | POWDER, FOR SUSPENSION | 60 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 42571-508-04 | 42571050804 | 9 g in 1 POUCH | 9 g | | | | Historical |
| 42571-508-29 | 42571050829 | 60 POUCH in 1 CARTON (42571-508-29) / 9 g in 1 POUCH (42571-508-04) | 60 pouch | 2026-04-01 | No | No | Current |