Potassium Chloride
- Product NDC
- 70518-2479
- 11-digit product format
- 705182479
- Labeler code
- 70518
- Product ID
- 70518-2479_e2a9d76e-b894-f522-e053-2995a90ae4e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- CAPSULE, COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203002
- Marketing category
- ANDA
- Marketing start
- 2019-12-12
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 10 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2479-0 | 70518247900 | 30 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2479-0) | | 2019-12-12 | 0000-00-00 | No | No | Current |
| 70518-2479-1 | 70518247901 | 100 POUCH in 1 BOX (70518-2479-1) > 1 CAPSULE, COATED, EXTENDED RELEASE in 1 POUCH (70518-2479-2) | 100 pouch | 2022-06-29 | 0000-00-00 | No | No | Current |