NDC 68382-538 – Potassium Citrate
Potassium Citrate 15 meq/1 · Tablet, Extended Release · Oral
Product NDC68382-538
Product details
- Brand name
- Potassium Citrate
- Generic name
- Potassium Citrate
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA203546
- Marketed since
- August 12, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-coagulant; Calculi Dissolution Agent
Active ingredients
- Potassium Citrate 15 meq/1
Uses, dosage, side effects and warnings for Potassium Citrate →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68382-538-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-538-01) | Aug 12, 2014 |
| 68382-538-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-538-05) | Aug 12, 2014 |
| 68382-538-06 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-538-06) | Aug 12, 2014 |
| 68382-538-10 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-538-10) | Aug 12, 2014 |
| 68382-538-16 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-538-16) | Aug 12, 2014 |
| 68382-538-30 | 10 BLISTER PACK in 1 CARTON (68382-538-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Aug 12, 2014 |
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