Potassium Chloride
- Product NDC
- 70518-0890
- 11-digit product format
- 705180890
- Labeler code
- 70518
- Product ID
- 70518-0890_e2965c7e-3c36-b11c-e053-2995a90a090c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076368
- Marketing category
- ANDA
- Marketing start
- 2017-12-08
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 20 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0890-0 | 70518089000 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-0890-0) | 2017-12-08 | 0000-00-00 | No | No | Current |
| 70518-0890-3 | 70518089003 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-0890-3) | 2019-07-09 | 0000-00-00 | No | No | Current |
| 70518-0890-4 | 70518089004 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-0890-4) | 2021-04-30 | 0000-00-00 | No | No | Current |