Potassium chloride extended release
- Product NDC
- 63629-8700
- 11-digit product format
- 636298700
- Labeler code
- 63629
- Product ID
- 63629-8700_e5479e84-3fba-4994-9bff-62492dc06969
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205993
- Marketing category
- ANDA
- Marketing start
- 2015-12-11
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 600 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
- 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 |
|---|
| 63629-8700-1 | 63629870001 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8700-1) | 2016-01-12 | 0000-00-00 | No | No | Current |