potassium chloride
- Product NDC
- 72603-337
- 11-digit product format
- 726030337
- Labeler code
- 72603
- Product ID
- 72603-337_fdab4887-b1a0-49d9-8bf4-07fd86ec6552
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA214422
- Marketing category
- ANDA
- Marketing start
- 2024-06-21
- Marketing end
- 2026-10-31
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- potassium chloride
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM CHLORIDE | 750 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 660YQ98I10 |
| Rxcui | 1801294, 1801298 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72603-337-01 | potassium chloride | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72603-337 | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [NORTHSTAR RX LLC] | 1 | Current NDC, 1 package rows | 20240622_b19a3fbf-cdbb-4f86-ac61-5dfb07e0a51a.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 |
|---|
| 72603-337-01 | 72603033701 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72603-337-01) | 2024-06-21 | 2026-10-31 | No | No | Historical |