Potassium-cit
- Product NDC
- 70518-3328
- 11-digit product format
- 705183328
- Labeler code
- 70518
- Product ID
- 70518-3328_d5653ac3-fbea-5a86-e053-2a95a90a5a99
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium-cit
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA214426
- Marketing category
- ANDA
- Marketing start
- 2022-01-11
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CITRATE
- Active strength
- 10 meq/1
- Pharmacologic classes
- Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]
- 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 |
|---|
| 70518-3328-0 | 70518332800 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3328-0) | 2022-01-11 | 0000-00-00 | No | No | Current |