Potassium Chloride
- Product NDC
- 60687-466
- 11-digit product format
- 606870466
- Labeler code
- 60687
- Product ID
- 60687-466_f0389da3-24f6-1045-e053-2995a90ae3c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- NDA018279
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-07-26
- Marketing end
- 2023-07-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-466-01 | 60687046601 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-466-01) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-466-11) | 100 blister pack | 2019-06-15 | 0000-00-00 | No | No | Current |