SEVELAMER CARBONATE
- Product NDC
- 72915-301
- 11-digit product format
- 729150301
- Labeler code
- 72915
- Product ID
- 72915-301_f2950e5a-8bb6-4ed2-8b5a-d5a2b37ad9fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SEVELAMER CARBONATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Anxin Pharma Inc.
- Application
- ANDA212970
- Marketing category
- ANDA
- Marketing start
- 2021-01-01
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72915-301-02 | 72915030102 | 30 TABLET, FILM COATED in 1 BOTTLE (72915-301-02) | 2021-01-01 | 0000-00-00 | No | No | Current |
| 72915-301-10 | 72915030110 | 180 TABLET, FILM COATED in 1 BOTTLE (72915-301-10) | 2021-01-01 | 0000-00-00 | No | No | Current |
| 72915-301-13 | 72915030113 | 270 TABLET, FILM COATED in 1 BOTTLE (72915-301-13) | 2021-01-01 | 0000-00-00 | No | No | Current |