Potassium Chloride
- Product NDC
- 70518-2313
- 11-digit product format
- 705182313
- Labeler code
- 70518
- Product ID
- 70518-2313_c8305db0-a433-e026-e053-2995a90aeefd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA019123
- Marketing category
- NDA
- Marketing start
- 2019-09-13
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2313 | POTASSIUM CHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [REMEDYREPACK INC.] | 7 | Legacy NDC | 20250311_99711cce-7e88-4adf-b0f8-245e8b8a62d6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2313-0 | 70518231300 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2313-0) | 2019-09-13 | 0000-00-00 | No | No | Current |
| 70518-2313-1 | 70518231301 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2313-1) | 2020-09-14 | 0000-00-00 | No | No | Current |