Sevelamer Carbonate
- Product NDC
- 70518-1102
- 11-digit product format
- 705181102
- Labeler code
- 70518
- Product ID
- 70518-1102_9022615d-cc0a-78ef-e053-2a95a90a1085
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sevelamer Carbonate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090975
- Marketing category
- ANDA
- Marketing start
- 2018-04-09
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record