Sevelamer carbonate
- Product NDC
- 16571-739
- 11-digit product format
- 165710739
- Labeler code
- 16571
- Product ID
- 16571-739_27857385-55ea-4630-a3ae-04df2812ed62
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sevelamer carbonate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rising Pharmaceuticals, Inc.
- Application
- ANDA204451
- Marketing category
- ANDA
- Marketing start
- 2020-12-16
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16571-739-03 | 16571073903 | 30 TABLET, FILM COATED in 1 BOTTLE (16571-739-03) | 2020-12-16 | 0000-00-00 | No | No | Current |
| 16571-739-27 | 16571073927 | 270 TABLET, FILM COATED in 1 BOTTLE (16571-739-27) | 2020-12-16 | 0000-00-00 | No | No | Current |