Potassium Chloride
- Product NDC
- 70166-582
- 11-digit product format
- 701660582
- Labeler code
- 70166
- Product ID
- 70166-582_bc2edad4-6442-1df2-e053-2995a90afe99
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Lohxa
- Application
- ANDA210041
- Marketing category
- ANDA
- Marketing start
- 2018-09-01
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 2 g/15mL
- Pharmacologic classes
- Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70166-582-15 | Potassium Chloride | 50 in 1 CARTON | SOLUTION | 50 | | 2 |
| 70166-582-15 | Potassium Chloride | 15 mL in 1 CUP, UNIT-DOSE | SOLUTION | 15 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70166-582 | POTASSIUM CHLORIDE SOLUTION [LOHXA] | 2 | Legacy NDC, 2 package rows | 20210227_843a7b4e-e549-4f29-8f1a-60671617a0c0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70166-582-15 | 70166058215 | 50 CUP, UNIT-DOSE in 1 CARTON (70166-582-15) > 15 mL in 1 CUP, UNIT-DOSE | 2019-01-01 | 0000-00-00 | No | No | Current |