POTASSIUM CHLORIDE
- Product NDC
- 70518-3384
- 11-digit product format
- 705183384
- Labeler code
- 70518
- Product ID
- 70518-3384_d9f1db05-4113-2a8f-e053-2a95a90ae0b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- POTASSIUM CHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA208864
- Marketing category
- ANDA
- Marketing start
- 2022-03-10
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 mg/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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 660YQ98I10 | POTASSIUM CHLORIDE | 7447-40-7 | POTASSIUM CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3384-0 | 70518338400 | 100 POUCH in 1 BOX (70518-3384-0) > 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-3384-1) | 100 pouch | 2022-03-10 | 0000-00-00 | No | No | Current |