colesevelam hydrochloride
- Product NDC
- 60687-621
- 11-digit product format
- 606870621
- Labeler code
- 60687
- Product ID
- 60687-621_cf2d97e0-30c7-2ad8-e053-2995a90aa8a4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- colesevelam hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA203480
- Marketing category
- ANDA
- Marketing start
- 2021-11-01
- Marketing end
- 0000-00-00
- Substance
- COLESEVELAM HYDROCHLORIDE
- Active strength
- 625 mg/1
- Pharmacologic classes
- Bile Acid Sequestrant [EPC],Bile-acid Binding Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 60687-621-25 | 60687062125 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-621-25) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-621-95) | 30 blister pack | 2021-11-01 | 0000-00-00 | No | No | Current |