Potassium Chloride
- Product NDC
- 27808-168
- 11-digit product format
- 278080168
- Labeler code
- 27808
- Product ID
- 27808-168_f15016a3-b389-4ca4-9127-f6f438254434
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Tris Pharma Inc
- Application
- ANDA214076
- Marketing category
- ANDA
- Marketing start
- 2022-01-26
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 20 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 | 20 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 |
|---|
| 27808-168-01 | Potassium Chloride | 473 mL in 1 BOTTLE | SOLUTION | 473 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 27808-168 | POTASSIUM CHLORIDE SOLUTION [TRIS PHARMA INC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20220612_159ddd0b-847e-4ecc-b3b2-9634cbb4dfa9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 27808-168-01 | 27808016801 | 473 mL in 1 BOTTLE (27808-168-01) | 473 ml | 2022-12-30 | 0000-00-00 | No | No | Current |