NDC 50090-7639 – Potassium Chloride
Potassium Chloride 750 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC50090-7639
Product details
- Brand name
- Potassium Chloride
- Generic name
- Potassium Chloride
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- NDA · NDA019123
- Marketed since
- April 17, 1986
- Listing expires
- December 31, 2026
- Pharmacologic class
- Osmotic Laxative; Potassium Salt
Active ingredients
- Potassium Chloride 750 mg/1
Uses, dosage, side effects and warnings for Potassium Chloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 50090-7639-0 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-0) | Aug 26, 2025 |
| 50090-7639-1 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-1) | Aug 26, 2025 |
| 50090-7639-2 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-2) | Aug 26, 2025 |
| 50090-7639-3 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-3) | Aug 26, 2025 |
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