NDC 70436-002 – Potassium Chloride
Potassium Chloride 750 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC70436-002
Product details
- Brand name
- Potassium Chloride
- Generic name
- Potassium Chloride
- Labeler
- Slate Run Pharmaceuticals, LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA209314
- Marketed since
- November 15, 2018
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 70436-002-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-002-01) | Nov 15, 2018 |
| 70436-002-02 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-002-02) | Nov 15, 2018 |
| 70436-002-03 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70436-002-03) | Nov 15, 2018 |
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