Potassium Chloride
- Product NDC
- 72789-239
- 11-digit product format
- 727890239
- Labeler code
- 72789
- Product ID
- 72789-239_dafc0a61-acc3-d91b-e053-2a95a90a328c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA212861
- Marketing category
- ANDA
- Marketing start
- 2020-05-11
- 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 Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-239 | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [PD-RX PHARMACEUTICALS, INC.] | 14 | Legacy NDC | 20240217_42937afb-8776-407e-a7b5-1fafd0a88344.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-239-30 | 72789023930 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-239-30) | 2022-03-24 | 0000-00-00 | No | No | Current |