Potassium Chloride
- Product NDC
- 68382-320
- 11-digit product format
- 683820320
- Labeler code
- 68382
- Product ID
- 68382-320_c3887ec5-c66d-4d1b-bab1-07bf0e8b3d47
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc
- Application
- NDA018279
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-06-01
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68382-320-01 | 2020-02-25 | C162847 | 48780-1 | 9d75b9d0-d411-f424-e053-dadaa90a57ce | 8d140d5e-a5d7-5302-3572-e606dd247410 |
| 68382-320-10 | 2020-02-25 | C162847 | 48780-1 | 9d75b9d0-d411-f424-e053-dadaa90a57ce | 8d140d5e-a5d7-5302-3572-e606dd247410 |
| 68382-320-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-d411-f424-e053-dadaa90a57ce | 8d140d5e-a5d7-5302-3572-e606dd247410 |
| 68382-320-10 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-d411-f424-e053-dadaa90a57ce | 8d140d5e-a5d7-5302-3572-e606dd247410 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68382-320-01 | EA - Each | 68382-320 | 72497685-ba01-4964-94ad-32be1a8bf7b2 | 1 | 2019-05-02 |
| 68382-320-10 | EA - Each | 68382-320 | d48b981a-2729-40b6-8d24-f6ddba7c3e7f | 1 | 2019-05-02 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 628953 | potassium chloride 10 MEQ (750 MG) Extended Release Oral Tablet | PSN | 418fa94a-9e92-4f06-b8c2-020c885e3412 | 4 |
| 628953 | potassium chloride 10 MEQ Extended Release Oral Tablet | SCD | 418fa94a-9e92-4f06-b8c2-020c885e3412 | 4 |
| 628953 | K+ Chloride 10 MEQ Extended Release Oral Tablet | SY | 418fa94a-9e92-4f06-b8c2-020c885e3412 | 4 |
| 628953 | Pot Chloride 10 MEQ Extended Release Oral Tablet | SY | 418fa94a-9e92-4f06-b8c2-020c885e3412 | 4 |
| 628953 | potassium chloride 750 MG (potassium 10 mEq) Extended Release Oral Tablet | SY | 418fa94a-9e92-4f06-b8c2-020c885e3412 | 4 |
| 628953 | potassium chloride 750 MG Extended Release Oral Tablet | SY | 418fa94a-9e92-4f06-b8c2-020c885e3412 | 4 |
| 628953 | potassium chloride 10 MEQ (750 MG) Extended Release Oral Tablet | PSN | 43e78f6e-a5a9-4c14-96cd-b28d7179adbf | 3 |
| 628953 | potassium chloride 10 MEQ Extended Release Oral Tablet | SCD | 43e78f6e-a5a9-4c14-96cd-b28d7179adbf | 3 |
| 628953 | K+ Chloride 10 MEQ Extended Release Oral Tablet | SY | 43e78f6e-a5a9-4c14-96cd-b28d7179adbf | 3 |
| 628953 | Pot Chloride 10 MEQ Extended Release Oral Tablet | SY | 43e78f6e-a5a9-4c14-96cd-b28d7179adbf | 3 |
| 628953 | potassium chloride 750 MG (potassium 10 mEq) Extended Release Oral Tablet | SY | 43e78f6e-a5a9-4c14-96cd-b28d7179adbf | 3 |
| 628953 | potassium chloride 750 MG Extended Release Oral Tablet | SY | 43e78f6e-a5a9-4c14-96cd-b28d7179adbf | 3 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 68382-320-01 | 68382032001 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-320-01) | 2017-06-01 | 0000-00-00 | No | No | Current |
| 68382-320-10 | 68382032010 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-320-10) | 2017-06-01 | 0000-00-00 | No | No | Current |