POTASSIUM CHLORIDE
- Product NDC
- 70518-3222
- 11-digit product format
- 705183222
- Labeler code
- 70518
- Product ID
- 70518-3222_cbfafd95-973b-d76a-e053-2995a90aade6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium CHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA214422
- Marketing category
- ANDA
- Marketing start
- 2021-09-14
- 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 |
|---|
| 70518-3222-0 | 70518322200 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3222-0) | 2021-09-14 | 0000-00-00 | No | No | Current |