Potassium Chloride
- Product NDC
- 63739-164
- 11-digit product format
- 637390164
- Labeler code
- 63739
- Product ID
- 63739-164_e26d6e45-b802-052d-e053-2a95a90ade6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- McKesson Corporation dba as SKY Packaging
- Application
- ANDA210766
- Marketing category
- ANDA
- Marketing start
- 2022-07-01
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 63739-164 | POTASSIUM CHLORIDE SOLUTION [MCKESSON CORPORATION DBA SKY PACKAGING] | 8 | Legacy NDC | 20250101_8823d4b5-3766-454d-912c-eec3b008ab09.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-164-34 | 63739016434 | 5 TRAY in 1 CASE (63739-164-34) > 10 CUP, UNIT-DOSE in 1 TRAY > 15 mL in 1 CUP, UNIT-DOSE (63739-164-74) | 5 tray | 2022-07-01 | 0000-00-00 | No | No | Current |