Potassium chloride extended release
- Product NDC
- 71205-996
- 11-digit product format
- 712050996
- Labeler code
- 71205
- Product ID
- 71205-996_21547c5d-6d3e-41c3-b426-2df82f01fbeb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA205993
- Marketing category
- ANDA
- Marketing start
- 2015-12-11
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 71205-996-00 | 71205099600 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-996-00) | 2019-12-19 | 0000-00-00 | No | No | Current |
| 71205-996-55 | 71205099655 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-996-55) | 2019-12-19 | 0000-00-00 | No | No | Current |
| 71205-996-65 | 71205099665 | 270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-996-65) | 2019-12-19 | 0000-00-00 | No | No | Current |
| 71205-996-78 | 71205099678 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-996-78) | 2019-12-19 | 0000-00-00 | No | No | Current |
| 71205-996-90 | 71205099690 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-996-90) | 2019-12-19 | 0000-00-00 | No | No | Current |
| 71205-996-97 | 71205099697 | 360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-996-97) | 2019-12-19 | 0000-00-00 | No | No | Current |