Potassium Chloride
- Product NDC
- 63187-610
- 11-digit product format
- 631870610
- Labeler code
- 63187
- Product ID
- 63187-610_38cd9d83-0fd6-47bb-82bc-629d7c974501
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA018279
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2011-02-22
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-610 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [PROFICIENT RX LP] | 3 | Legacy NDC | 20191121_956e602f-772d-441e-9bf5-d1560c5b9615.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-610-00 | 63187061000 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-610-00) | 2018-12-01 | 0000-00-00 | No | No | Current |
| 63187-610-30 | 63187061030 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-610-30) | 2018-12-01 | 0000-00-00 | No | No | Current |
| 63187-610-60 | 63187061060 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-610-60) | 2018-12-01 | 0000-00-00 | No | No | Current |
| 63187-610-90 | 63187061090 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-610-90) | 2018-12-01 | 0000-00-00 | No | No | Current |