Sevelamer Carbonate
- Product NDC
- 70518-2490
- 11-digit product format
- 705182490
- Labeler code
- 70518
- Product ID
- 70518-2490_c9b0275c-cb30-59ed-e053-2a95a90a01ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sevelamer Carbonate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA022127
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-12-17
- Marketing end
- 0000-00-00
- Substance
- SEVELAMER CARBONATE
- Active strength
- 800 mg/1
- Pharmacologic classes
- Phosphate Binder [EPC],Phosphate Chelating 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2490-0 | 70518249000 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2490-0) | 2019-12-17 | 0000-00-00 | No | No | Current |