Potassium Chloride
- Product NDC
- 71335-1210
- 11-digit product format
- 713351210
- Labeler code
- 71335
- Product ID
- 71335-1210_b38e868e-7d50-45ac-b782-0d96ff53a5c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-1210-1 | Potassium Chloride | 180 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 180 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-1210 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK] | 4 | Legacy NDC, 1 package rows | 20200919_418fa94a-9e92-4f06-b8c2-020c885e3412.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 |
|---|
| 71335-1210-1 | 71335121001 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1210-1) | 2019-05-09 | 0000-00-00 | No | No | Current |