NDC 65862-987 – Potassium Chloride
Potassium Chloride 750 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC65862-987
Product details
- Brand name
- Potassium Chloride
- Generic name
- Potassium Chloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210921
- Marketed since
- December 19, 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 65862-987-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-987-01) | Dec 19, 2018 |
| 65862-987-12 | 120 BLISTER PACK in 1 CARTON (65862-987-12) / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-987-06) | Dec 19, 2018 |
| 65862-987-80 | 80 BLISTER PACK in 1 CARTON (65862-987-80) / 4 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-987-04) | Dec 19, 2018 |
| 65862-987-99 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-987-99) | Dec 19, 2018 |
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