Sevelamer carbonate
- Product NDC
- 69097-967
- 11-digit product format
- 690970967
- Labeler code
- 69097
- Product ID
- 69097-967_444a974f-7f31-4b53-93c9-f5b9a251f711
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SEVELAMER CARBONATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cipla USA Inc.
- Application
- ANDA203860
- Marketing category
- ANDA
- Marketing start
- 2017-10-26
- 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 |
|---|
| 69097-967-93 | Sevelamer carbonate | 270 in 1 BOTTLE | TABLET, FILM COATED | 270 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69097-967 | SEVELAMER CARBONATE TABLET, FILM COATED [CIPLA USA INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20230119_134f32c1-b5d5-44d0-9da5-85033e99320a.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 |
|---|
| 69097-967-93 | 69097096793 | 270 TABLET, FILM COATED in 1 BOTTLE (69097-967-93) | 2019-08-08 | 0000-00-00 | No | No | Current |