Potassium Chloride
- Product NDC
- 63187-979
- 11-digit product format
- 631870979
- Labeler code
- 63187
- Product ID
- 63187-979_2e3dc23e-8c5d-4c9c-878d-decc75c85677
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA019123
- Marketing category
- NDA
- Marketing start
- 1986-04-17
- 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 |
|---|
| 63187-979 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [PROFICIENT RX LP] | 3 | Legacy NDC | 20191105_034d279c-05e4-496e-9fc6-058dae158c60.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-979-30 | 63187097930 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-979-30) | 2018-02-01 | 0000-00-00 | No | No | Current |
| 63187-979-60 | 63187097960 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-979-60) | 2018-02-01 | 0000-00-00 | No | No | Current |
| 63187-979-90 | 63187097990 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-979-90) | 2018-02-01 | 0000-00-00 | No | No | Current |