Potassium Chloride
- Product NDC
- 50090-4285
- 11-digit product format
- 500904285
- Labeler code
- 50090
- Product ID
- 50090-4285_8af0b42b-c4ff-4cf2-9793-8333ff6ed36b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA018279
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-06-01
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 mg/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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4285-0 | 50090428500 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4285-0) | 2019-04-30 | 0000-00-00 | No | No | Current |
| 50090-4285-1 | 50090428501 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4285-1) | 2019-04-30 | 0000-00-00 | No | No | Current |
| 50090-4285-2 | 50090428502 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4285-2) | 2019-04-30 | 0000-00-00 | No | No | Current |
| 50090-4285-3 | 50090428503 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4285-3) | 2019-04-30 | 0000-00-00 | No | No | Current |