NDC 60687-810 – Potassium Chloride
Potassium Chloride 750 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC60687-810
Product details
- Brand name
- Potassium Chloride
- Generic name
- Potassium Chloride
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210921
- Marketed since
- January 20, 2024
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 60687-810-09 | 80 BLISTER PACK in 1 CARTON (60687-810-09) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-810-11) | Jan 20, 2024 |
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