Potassium Chloride
- Product NDC
- 67296-1653
- 11-digit product format
- 672961653
- Labeler code
- 67296
- Product ID
- 67296-1653_b8df8259-aeca-dee4-e053-2995a90aa87b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- NDA019123
- Marketing category
- NDA
- Marketing start
- 2019-01-01
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1653-3 | Potassium Chloride | 30 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1653 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [REDPHARM DRUG, INC.] | 2 | Legacy NDC, 1 package rows | 20210115_89095e99-121b-2fb9-e053-2995a90ac7fb.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 |
|---|
| 67296-1653-3 | 67296165303 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67296-1653-3) | 2019-01-01 | 0000-00-00 | No | No | Current |