Cholestyramine
- Product NDC
- 62559-620
- 11-digit product format
- 625590620
- Labeler code
- 62559
- Product ID
- 62559-620_80689b75-ec08-4723-8e8b-4da8780e73de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cholestyramine
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA074554
- Marketing category
- ANDA
- Marketing start
- 2018-06-26
- 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 |
|---|
| 62559-620-37 | 62559062037 | 378 g in 1 CAN (62559-620-37) | 378 g | 2018-06-26 | 0000-00-00 | No | No | Current |