NDC 68462-357 – Potassium Chloride
Potassium Chloride 750 mg/1 · Capsule, Extended Release · Oral
Product NDC68462-357
Product details
- Brand name
- Potassium Chloride
- Generic name
- Potassium Chloride
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202868
- Marketed since
- January 20, 2016
- 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 |
|---|---|---|
| 68462-357-01 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-01) | Jan 20, 2016 |
| 68462-357-05 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-05) | Jan 20, 2016 |
| 68462-357-90 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-90) | Jun 1, 2016 |
Recalls mentioning this NDC
- D-0606-2024 Jul 24, 2024 · Class II
CGMP Deviations - D-0605-2024 Jul 24, 2024 · Class I
Failed Dissolution Specifications - D-0607-2024 Jul 24, 2024 · Class II
CGMP Deviations - D-0604-2024 Jul 24, 2024 · Class I
Failed Dissolution Specifications
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