Potassium Chloride
- Product NDC
- 63739-973
- 11-digit product format
- 637390973
- Labeler code
- 63739
- Product ID
- 63739-973_e2757913-042b-7d52-e053-2995a90aa53b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Mckesson Corporation DBA SKY Packaginng
- Application
- ANDA074726
- Marketing category
- ANDA
- Marketing start
- 1998-11-20
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 1500 mg/1
- 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 Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63739-973-10 | Potassium Chloride | 10 in 1 BOX, UNIT-DOSE | TABLET, EXTENDED RELEASE | 10 | | 7 |
| 63739-973-10 | Potassium Chloride | 10 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 10 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-973 | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [MCKESSON CORPORATION DBA SKY PACKAGINNG] | 7 | Legacy NDC, 2 package rows | 20250112_5cccc39f-6a6d-415e-a55f-f4ee57f72a0a.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 |
|---|
| 63739-973-10 | 63739097310 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-973-10) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 10 blister pack | 1998-11-20 | 0000-00-00 | No | No | Current |