Potassium Chloride
- Product NDC
- 53808-1125
- 11-digit product format
- 538081125
- Labeler code
- 53808
- Product ID
- 53808-1125_3b28d822-0887-4701-81ff-8002d3b475d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- DOH CENTRAL PHARMACY
- Application
- ANDA204662
- Marketing category
- ANDA
- Marketing start
- 2018-05-24
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 10 meq/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
- 2020-12-31
- 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 |
|---|
| 53808-1125-1 | Potassium Chloride | 30 in 1 BLISTER PACK | TABLET, FILM COATED, EXTENDED RE | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-1125 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [DOH CENTRAL PHARMACY] | 1 | Legacy NDC, 1 package rows | 20190125_b917235f-7989-4570-9532-fc5ff0468784.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 |
|---|
| 53808-1125-1 | 53808112501 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (53808-1125-1) | 2018-05-24 | 0000-00-00 | No | No | Current |