Sevelamer carbonate
- Product NDC
- 70518-0909
- 11-digit product format
- 705180909
- Labeler code
- 70518
- Product ID
- 70518-0909_8f096f20-b567-4b6c-e053-2a95a90a5cc4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SEVELAMER CARBONATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203860
- Marketing category
- ANDA
- Marketing start
- 2017-12-14
- 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