potassium chloride
- Product NDC
- 68382-854
- 11-digit product format
- 683820854
- Labeler code
- 68382
- Product ID
- 68382-854_37302db1-d7cc-4b79-8b3e-f14d40342ef4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA208445
- Marketing category
- ANDA
- Marketing start
- 2019-06-30
- 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
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- potassium chloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM CHLORIDE | 750 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 660YQ98I10 |
| Rxcui | 312504, 315183 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68382-854-01 | potassium chloride | 100 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 100 | | 3 |
| 68382-854-05 | potassium chloride | 500 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 500 | | 3 |
| 68382-854-10 | potassium chloride | 1000 in 1 BOTTLE | CAPSULE, EXTENDED RELEASE | 1000 | | 3 |
| 68382-854-30 | potassium chloride | 10 in 1 BLISTER PACK | CAPSULE, EXTENDED RELEASE | 10 | | 3 |
| 68382-854-77 | potassium chloride | 10 in 1 CARTON | CAPSULE, EXTENDED RELEASE | 10 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68382-854 | POTASSIUM CHLORIDE CAPSULE, EXTENDED RELEASE [ZYDUS PHARMACEUTICALS (USA) INC.] | 3 | Current NDC, Legacy NDC, 5 package rows | 20210209_51586c47-1aff-4ce6-8030-89f9eb1bc9ac.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68382-854-01 | 68382085401 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-854-01) | | 2019-06-30 | 0000-00-00 | No | No | Current |
| 68382-854-05 | 68382085405 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-854-05) | | 2019-06-30 | 0000-00-00 | No | No | Current |
| 68382-854-10 | 68382085410 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-854-10) | | 2019-06-30 | 0000-00-00 | No | No | Current |
| 68382-854-30 | 68382085430 | 10 in 1 BLISTER PACK | | | | | | Historical |
| 68382-854-77 | 68382085477 | 10 BLISTER PACK in 1 CARTON (68382-854-77) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68382-854-30) | 10 blister pack | 2019-06-30 | 0000-00-00 | No | No | Current |