Potassium Chloride for Oral Solution
- Product NDC
- 10135-820
- 11-digit product format
- 101350820
- Labeler code
- 10135
- Product ID
- 10135-820_3e780042-e8cd-95fc-e063-6294a90aa28a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride for Oral Solution
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Marlex Pharmaceuticals Inc
- Application
- ANDA212183
- Marketing category
- ANDA
- Marketing start
- 2025-08-01
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 3 g/4.75g
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Potassium Chloride for Oral Solution
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM CHLORIDE | 3 g/4.75g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 660YQ98I10 |
| Rxcui | 312515, 314182 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10135-820-08 | Potassium Chloride for Oral Solution | 3 g in 1 BOTTLE | SOLUTION | 3 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 10135-820-08 | 10135082008 | 3 g in 1 BOTTLE (10135-820-08) | 3 g | 2025-08-01 | No | No | Historical |