cholestyramine powder for suspension
- Product NDC
- 63629-9197
- 11-digit product format
- 636299197
- Labeler code
- 63629
- Product ID
- 63629-9197_8efe779f-a75f-43b4-90ea-836e2a45470b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cholestyramine powder for suspension
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211856
- Marketing category
- ANDA
- Marketing start
- 2021-10-20
- Marketing end
- 0000-00-00
- Substance
- CHOLESTYRAMINE
- Active strength
- 4 g/8.78g
- 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 |
|---|
| 63629-9197-1 | 63629919701 | 60 POUCH in 1 CARTON (63629-9197-1) > 8.78 g in 1 POUCH | 60 pouch | 2022-03-02 | 0000-00-00 | No | No | Current |