Cholestyramine
- Product NDC
- 63629-2163
- 11-digit product format
- 636292163
- Labeler code
- 63629
- Product ID
- 63629-2163_9268b1c8-83f6-41c9-a560-274ced198248
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cholestyramine
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077204
- Marketing category
- ANDA
- Marketing start
- 2005-09-15
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2163-1 | 63629216301 | 60 PACKET in 1 CARTON (63629-2163-1) > 9 g in 1 PACKET | 60 packet | 2021-05-21 | 0000-00-00 | No | No | Current |