Potassium Chloride
- Product NDC
- 71335-0763
- 11-digit product format
- 713350763
- Labeler code
- 71335
- Product ID
- 71335-0763_bd725eed-d711-4624-ac86-c99034016e01
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA019123
- Marketing category
- NDA
- Marketing start
- 1986-04-17
- Marketing end
- 2022-02-28
- 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
- 0000-00-00
- 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 |
|---|
| 71335-0763-1 | 71335076301 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0763-1) | 2021-12-27 | 2022-02-28 | No | No | Current |
| 71335-0763-2 | 71335076302 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0763-2) | 2021-12-27 | 2022-02-28 | No | No | Current |
| 71335-0763-3 | 71335076303 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0763-3) | 2018-04-04 | 2022-02-28 | No | No | Current |