Potassium Citrate
- Product NDC
- 72162-1758
- 11-digit product format
- 721621758
- Labeler code
- 72162
- Product ID
- 72162-1758_d89425f2-a782-4b9d-851c-8729be85ecca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Citrate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212779
- Marketing category
- ANDA
- Marketing start
- 2020-03-16
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Potassium Citrate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM CITRATE | 10 meq/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | EE90ONI6FF |
| Rxcui | 199381 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1758-1 | Potassium Citrate | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1758 | POTASSIUM CITRATE TABLET, EXTENDED RELEASE [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240208_595343aa-b760-4158-9c49-dd5368f45e2c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1758-1 | 72162175801 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1758-1) | 2026-03-25 | No | No | Historical |