Drug application
MICRO-K LS (POTASSIUM CHLORIDE)
Drugs@FDA NDA 019561 · KV PHARM
Key facts
| Drug name | MICRO-K LS |
|---|---|
| Active ingredients | POTASSIUM CHLORIDE |
| Application type | NDA |
| Application number | 019561 |
| Company | KV PHARM |
| Dosage forms | FOR SUSPENSION, EXTENDED RELEASE, ORAL |
| Strength | 20MEQ/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
| Marketing status | Discontinued |
| Reference listed drug | Yes |
| Latest submission class | Type 3 - New Dosage Form |
| Latest submission status date | Aug 26, 1988 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- None Therapeutic equivalents
- No FDA letters on file
- Yes FDA reviews on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: