Sevelamer carbonate
- Product NDC
- 50436-0893
- 11-digit product format
- 504360893
- Labeler code
- 50436
- Product ID
- 50436-0893_aaf0e9d0-7018-4e7b-ad80-95d6ff96aa11
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SEVELAMER CARBONATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA203860
- Marketing category
- ANDA
- Marketing start
- 2017-10-26
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-0893-1 | Sevelamer carbonate | 1 in 1 POUCH | TABLET, FILM COATED | 1 | | 2 |
| 50436-0893-1 | Sevelamer carbonate | 50 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0893 | SEVELAMER CARBONATE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | Legacy NDC, 2 package rows | 20180403_0883b9aa-8562-486c-9ab7-9f82f71015fe.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0893-1 | 50436089301 | 1 in 1 POUCH | Historical |