Sevelamer Carbonate
- Product NDC
- 16714-814
- 11-digit product format
- 167140814
- Labeler code
- 16714
- Product ID
- 16714-814_a2199a9d-47ad-4994-ba6f-af6e4d1ad7da
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sevelamer Carbonate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA207179
- Marketing category
- ANDA
- Marketing start
- 2018-06-06
- Substance
- SEVELAMER CARBONATE
- Active strength
- 800 mg/1
- Pharmacologic classes
- Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sevelamer Carbonate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SEVELAMER CARBONATE | 800 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9YCX42I8IU |
| Rxcui | 749206 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 16714-814-01 | Sevelamer Carbonate | 270 in 1 BOTTLE | TABLET, FILM COATED | 270 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16714-814 | SEVELAMER CARBONATE TABLET, FILM COATED [NORTHSTAR RX LLC] | 11 | Current NDC, Legacy NDC, 1 package rows | 20240425_9b4d0720-f4e7-4b4f-affc-57ce8bb0b722.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-814-01 | 16714081401 | 270 TABLET, FILM COATED in 1 BOTTLE (16714-814-01) | 2018-06-06 | 0000-00-00 | No | No | Current |