POTASSIUM CHLORIDE
- Product NDC
- 43602-285
- 11-digit product format
- 436020285
- Labeler code
- 43602
- Product ID
- 43602-285_ddde8a6a-992e-4bc4-9fc6-da9dfc08e092
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Ascent Pharmaceuticals, Inc.
- Application
- ANDA214422
- Marketing category
- ANDA
- Marketing start
- 2020-12-30
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 1500 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43602-285 | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [ASCENT PHARMACEUTICALS, INC.] | 3 | Legacy NDC | 20210108_c47c0704-26f1-41ba-8af6-50250686d612.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43602-285-05 | 43602028505 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43602-285-05) | 2020-12-30 | 0000-00-00 | No | No | Current |
| 43602-285-30 | 43602028530 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43602-285-30) | 2020-12-30 | 0000-00-00 | No | No | Current |