Potassium Chloride
- Product NDC
- 53041-680
- 11-digit product format
- 530410680
- Labeler code
- 53041
- Product ID
- 53041-680_859606e1-12d2-4eff-b6f3-4fa59c4da89b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Guardian Drug Company
- Application
- ANDA214892
- Marketing category
- ANDA
- Marketing start
- 2021-07-09
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 40 meq/15mL
- 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
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM CHLORIDE | 40 meq/15mL |
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 |
|---|
| 53041-680-06 | Potassium Chloride | 473 mL in 1 BOTTLE | SOLUTION | 473 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53041-680 | POTASSIUM CHLORIDE SOLUTION [GUARDIAN DRUG COMPANY] | 3 | Current NDC, 1 package rows | 20230117_3d460e84-27a0-485c-8b11-58d03d9064aa.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 53041-680-06 | 53041068006 | 473 mL in 1 BOTTLE (53041-680-06) | 473 ml | 2021-07-09 | No | No | Current |