Potassium Chloride
- Product NDC
- 63629-8115
- 11-digit product format
- 636298115
- Labeler code
- 63629
- Product ID
- 63629-8115_61f0825c-83ee-4558-a73f-81dc163d4a36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210733
- Marketing category
- ANDA
- Marketing start
- 2018-08-31
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 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
- 2020-12-31
- 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 |
|---|
| 63629-8115-1 | 63629811501 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8115-1) | 2019-07-18 | 0000-00-00 | No | No | Current |