Potassium Chloride
- Product NDC
- 63187-668
- 11-digit product format
- 631870668
- Labeler code
- 63187
- Product ID
- 63187-668_5069666b-6a49-4e5c-80a5-e3cc4b921cc0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA076368
- Marketing category
- ANDA
- Marketing start
- 2004-08-18
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 20 meq/1
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63187-668 | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [PROFICIENT RX LP] | 7 | Legacy NDC | 20230225_70d3497a-1144-47f2-a924-aec8a9881dbd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-668-03 | 63187066803 | 3 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-668-03) | 2017-05-01 | 0000-00-00 | No | No | Current |
| 63187-668-10 | 63187066810 | 10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-668-10) | 2017-03-01 | 0000-00-00 | No | No | Current |
| 63187-668-30 | 63187066830 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-668-30) | 2016-03-01 | 0000-00-00 | No | No | Current |
| 63187-668-60 | 63187066860 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-668-60) | 2016-03-01 | 0000-00-00 | No | No | Current |
| 63187-668-90 | 63187066890 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-668-90) | 2016-03-01 | 0000-00-00 | No | No | Current |