Potassium Chloride Extended-release
- Product NDC
- 70518-3521
- 11-digit product format
- 705183521
- Labeler code
- 70518
- Product ID
- 70518-3521_eadc37d2-a00c-5af2-e053-2a95a90a7f59
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride Extended-release
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA214452
- Marketing category
- ANDA
- Marketing start
- 2022-09-14
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 1500 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3521 | POTASSIUM CHLORIDE EXTENDED-RELEASE TABLET [REMEDYREPACK INC.] | 3 | Legacy NDC | 20240116_d56509d3-e6b9-4070-b009-da057c6513c4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3521-0 | 70518352100 | 30 TABLET in 1 BLISTER PACK (70518-3521-0) | 30 tablet | 2022-09-14 | 0000-00-00 | No | No | Current |