Potassium Chloride
- Product NDC
- 71335-2447
- 11-digit product format
- 713352447
- Labeler code
- 71335
- Product ID
- 71335-2447_ca9361cb-0e2a-4a78-9eb2-e45b7cfc3bb6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209688
- Marketing category
- ANDA
- Marketing start
- 2023-04-10
- 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
- 2026-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 71335-2447_ca9361cb-0e2a-4a78-9eb2-e45b7cfc3bb6
- SPL ID
- ca9361cb-0e2a-4a78-9eb2-e45b7cfc3bb6
- Product type
- HUMAN PRESCRIPTION DRUG
- Finished product
- Yes
- Brand name base
- Potassium Chloride
- Brand name suffix
- Extended-Release
- Generic name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing start
- 2023-04-10
- Marketing category
- ANDA
- Application number
- ANDA209688
- 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]
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| POTASSIUM CHLORIDE | 750 mg/1 |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 660YQ98I10 |
| Rxcui | 628953 |
| Spl Set Id | 8bae6f0f-58ca-490f-a725-8ec4bc6ba514 |
| Manufacturer Name | Bryant Ranch Prepack |
openFDA Package Details
| Package NDC | Description | Marketing start | Sample |
|---|
| 71335-2447-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-1) | 2024-09-18 | No |
| 71335-2447-2 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-2) | 2024-09-18 | No |
| 71335-2447-3 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-3) | 2024-09-18 | No |
| 71335-2447-4 | 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-4) | 2024-09-18 | No |
| 71335-2447-5 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-5) | 2024-09-18 | No |
| 71335-2447-6 | 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-6) | 2024-09-18 | No |
| 71335-2447-7 | 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-7) | 2024-09-18 | No |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 660YQ98I10 | POTASSIUM CHLORIDE | 7447-40-7 | POTASSIUM CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2447-1 | 71335244701 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-1) | 2024-09-18 | No | No | Historical |
| 71335-2447-2 | 71335244702 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-2) | 2024-09-18 | No | No | Historical |
| 71335-2447-3 | 71335244703 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-3) | 2024-09-18 | No | No | Historical |
| 71335-2447-4 | 71335244704 | 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-4) | 2024-09-18 | No | No | Historical |
| 71335-2447-5 | 71335244705 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-5) | 2024-09-18 | No | No | Historical |
| 71335-2447-6 | 71335244706 | 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-6) | 2024-09-18 | No | No | Historical |
| 71335-2447-7 | 71335244707 | 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-7) | 2024-09-18 | No | No | Historical |