POTASSIUM CITRATE
- Product NDC
- 72162-2120
- 11-digit product format
- 721622120
- Labeler code
- 72162
- Product ID
- 72162-2120_29ad8572-bd95-44f4-a554-307431397d2d
- 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
- 10 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| EE90ONI6FF | POTASSIUM CITRATE | 6100-05-6 | POTASSIUM CITRATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2120-1 | 72162212001 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2120-1) | 2023-09-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| POTASSIUM CITRATE | Bryant Ranch Prepack | 2023-09-15 | HUMAN PRESCRIPTION DRUG LABEL | 100 |