Sevelamer Carbonate
- Product NDC
- 71205-966
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sevelamer Carbonate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA200959
- Marketing category
- ANDA
- Substance
- SEVELAMER CARBONATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-966-67 | 270 TABLET, FILM COATED in 1 BOTTLE (71205-966-67) | 2020-06-09 | 2027-11-30 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sevelamer Carbonate | Proficient Rx LP | 2024-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 3 |