Potassium Chloride
- Product NDC
- 60505-6185
- 11-digit product format
- 605056185
- Labeler code
- 60505
- Product ID
- 60505-6185_e8d857f5-2895-b451-3566-14ba9b508460
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Apotex Corp
- Application
- ANDA211067
- Marketing category
- ANDA
- Marketing start
- 2021-10-07
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60505-6185 | POTASSIUM CHLORIDE SOLUTION [APOTEX CORP] | 12 | Legacy NDC | 20250523_18ab4157-e99a-bff3-9ef8-9bb5c32ca36b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-6185-6 | 60505618506 | 1 BOTTLE, PLASTIC in 1 CARTON (60505-6185-6) > 473 mL in 1 BOTTLE, PLASTIC | 2021-10-07 | 0000-00-00 | No | No | Current |