potassium chloride
- Product NDC
- 68001-445
- 11-digit product format
- 680010445
- Labeler code
- 68001
- Product ID
- 68001-445_83d51a49-303a-40a3-ba48-43c45dc865cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA203562
- Marketing category
- ANDA
- Marketing start
- 2020-10-02
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 1500 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
- 2021-12-31
- 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 |
|---|
| 68001-445-00 | 68001044500 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-445-00) | 2020-10-02 | 0000-00-00 | No | No | Current |
| 68001-445-03 | 68001044503 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-445-03) | 2020-10-02 | 0000-00-00 | No | No | Current |