Potassium Chloride
- Product NDC
- 43826-025
- 11-digit product format
- 438260025
- Labeler code
- 43826
- Product ID
- 43826-025_f1e24735-dec2-ec06-e053-2a95a90af1b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bora Pharmaceutical Laboratories Inc.
- Application
- ANDA209688
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- 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
- 2024-12-31
- 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 |
|---|
| 43826-025-01 | 43826002501 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43826-025-01) | 2020-07-01 | 0000-00-00 | No | No | Current |
| 43826-025-07 | 43826002507 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43826-025-07) | 2020-07-01 | 0000-00-00 | No | No | Current |