COLESTIPOL HYDROCHLORIDE
- Product NDC
- 70518-2693
- 11-digit product format
- 705182693
- Labeler code
- 70518
- Product ID
- 70518-2693_ccfc1b30-f487-d6ab-e053-2995a90ad673
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- COLESTIPOL HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077510
- Marketing category
- ANDA
- Marketing start
- 2020-04-15
- Marketing end
- 0000-00-00
- Substance
- COLESTIPOL HYDROCHLORIDE
- Active strength
- 1 g/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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2693-0 | 70518269300 | 30 POUCH in 1 BOX (70518-2693-0) > 1 TABLET, FILM COATED in 1 POUCH (70518-2693-1) | 30 pouch | 2020-04-15 | 0000-00-00 | No | No | Current |