Potassium Chloride
- Product NDC
- 71335-1315
- 11-digit product format
- 713351315
- Labeler code
- 71335
- Product ID
- 71335-1315_c60c0f9a-e6fe-48b1-bc62-95a3caf9b99f
- 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 |
|---|
| 71335-1315-1 | Potassium Chloride | 30 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 30 | | 3 |
| 71335-1315-2 | Potassium Chloride | 60 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 60 | | 3 |
| 71335-1315-3 | Potassium Chloride | 90 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 90 | | 3 |
| 71335-1315-4 | Potassium Chloride | 15 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 15 | | 3 |
| 71335-1315-5 | Potassium Chloride | 180 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 180 | | 3 |
| 71335-1315-6 | Potassium Chloride | 28 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 28 | | 3 |
| 71335-1315-7 | Potassium Chloride | 10 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 10 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-1315 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK] | 3 | Legacy NDC, 7 package rows | 20200919_43e78f6e-a5a9-4c14-96cd-b28d7179adbf.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 |
|---|
| 71335-1315-1 | 71335131501 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-1) | 2019-08-27 | 0000-00-00 | No | No | Current |
| 71335-1315-2 | 71335131502 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-2) | 2019-08-27 | 0000-00-00 | No | No | Current |
| 71335-1315-3 | 71335131503 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-3) | 2019-08-27 | 0000-00-00 | No | No | Current |
| 71335-1315-4 | 71335131504 | 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-4) | 2019-08-27 | 0000-00-00 | No | No | Current |
| 71335-1315-5 | 71335131505 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-5) | 2019-08-27 | 0000-00-00 | No | No | Current |
| 71335-1315-6 | 71335131506 | 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-6) | 2019-08-27 | 0000-00-00 | No | No | Current |
| 71335-1315-7 | 71335131507 | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1315-7) | 2019-08-27 | 0000-00-00 | No | No | Current |