potassium chloride
- Product NDC
- 70518-2234
- 11-digit product format
- 705182234
- Labeler code
- 70518
- Product ID
- 70518-2234_c716744f-f398-1c5d-e053-2a95a90afd23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203562
- Marketing category
- ANDA
- Marketing start
- 2019-07-25
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2234-0 | 70518223400 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2234-0) | 2019-07-25 | 0000-00-00 | No | No | Current |