NDC 33342-418 – Potassium chloride
Potassium Chloride 750 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC33342-418
Product details
- Brand name
- Potassium chloride
- Generic name
- Potassium chloride
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA212987
- Marketed since
- September 8, 2024
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 33342-418-11 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-418-11) | Sep 8, 2024 |
| 33342-418-12 | 10 BLISTER PACK in 1 CARTON (33342-418-12) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Sep 8, 2024 |
| 33342-418-15 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-418-15) | Sep 8, 2024 |
| 33342-418-34 | 10 BLISTER PACK in 1 CARTON (33342-418-34) / 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | Sep 8, 2024 |
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