Potassium Chloride
- Product NDC
- 70518-3525
- 11-digit product format
- 705183525
- Labeler code
- 70518
- Product ID
- 70518-3525_e9073447-9989-6f35-e053-2a95a90ae44c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA212861
- Marketing category
- ANDA
- Marketing start
- 2022-09-17
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3525 | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [REMEDYREPACK INC.] | 4 | Legacy NDC | 20240323_4270cce8-4cbb-4d67-a4cb-f073ef554d12.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3525-0 | 70518352500 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3525-0) | 2022-09-17 | 0000-00-00 | No | No | Current |