POTASSIUM CITRATE
- Product NDC
- 71335-2897
- 11-digit product format
- 713352897
- Labeler code
- 71335
- Product ID
- 71335-2897_41d908e6-82e7-3ae6-e063-6294a90aeb03
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Citrate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA214420
- Marketing category
- ANDA
- Marketing start
- 2021-02-15
- Substance
- POTASSIUM CITRATE
- Active strength
- 15 meq/1
- Pharmacologic classes
- Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- POTASSIUM CITRATE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM CITRATE | 15 meq/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | EE90ONI6FF |
| Rxcui | 898490 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2897-1 | POTASSIUM CITRATE | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2897-1 | 71335289701 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2897-1) | 2025-10-23 | No | No | Current |