NDC 68382-861 – Potassium Chloride
Potassium Chloride 750 mg/1 · Tablet, Extended Release · Oral
Product NDC68382-861
Product details
- Brand name
- Potassium Chloride
- Generic name
- Potassium Chloride
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210395
- Marketed since
- February 3, 2022
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 68382-861-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-861-01) | Feb 3, 2022 |
| 68382-861-10 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-861-10) | Feb 3, 2022 |
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