SEVELAMER CARBONATE
- Product NDC
- 69680-143
- 11-digit product format
- 696800143
- Labeler code
- 69680
- Product ID
- 69680-143_56ec6273-334f-4b70-ad1e-fd98255a55a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SEVELAMER CARBONATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Vitruvias Therapeutics
- Application
- ANDA212970
- Marketing category
- ANDA
- Marketing start
- 2021-02-15
- 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 |
|---|
| 69680-143-30 | 69680014330 | 30 TABLET, FILM COATED in 1 BOTTLE (69680-143-30) | 2021-02-15 | 0000-00-00 | No | No | Current |
| 69680-143-92 | 69680014392 | 180 TABLET, FILM COATED in 1 BOTTLE (69680-143-92) | 2021-02-15 | 0000-00-00 | No | No | Current |
| 69680-143-95 | 69680014395 | 270 TABLET, FILM COATED in 1 BOTTLE (69680-143-95) | 2021-02-15 | 0000-00-00 | No | No | Current |