Potassium Chloride
- Product NDC
- 51655-585
- 11-digit product format
- 516550585
- Labeler code
- 51655
- Product ID
- 51655-585_6c70ed2b-67cd-4dd5-a5dc-524c4d95475f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals, LLC
- Application
- ANDA076368
- Marketing category
- ANDA
- Marketing start
- 2014-10-22
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 20 meq/1
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-585 | POTASSIUM CHLORIDE ER (POTASSIUM CHLORIDE) TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 1 | Legacy NDC | 20141031_a528e2ff-f636-4c3a-959b-2b33d2f501c3.zip |