Cholestyramine Light
- Product NDC
- 56156-001
- 11-digit product format
- 561560001
- Labeler code
- 56156
- Product ID
- 56156-001_b67331c5-f17a-8904-e053-2995a90a858c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cholestyramine
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Laboratorios Rubio SA
- Application
- ANDA209599
- Marketing category
- ANDA
- Marketing start
- 2020-11-12
- Marketing end
- 0000-00-00
- Substance
- CHOLESTYRAMINE
- Active strength
- 4 g/4.8g
- Pharmacologic classes
- Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 56156-001-10 | 56156000110 | 201.6 g in 1 CAN (56156-001-10) | 201.6 g | 2020-11-12 | 0000-00-00 | No | No | Current |
| 56156-001-20 | 56156000120 | 60 POUCH in 1 CARTON (56156-001-20) > 4.8 g in 1 POUCH | 60 pouch | 2020-11-12 | 0000-00-00 | No | No | Current |