NDC 64380-861 – Potassium Chloride
Potassium Chloride 750 mg/1 · Tablet, Extended Release · Oral
Product NDC64380-861
Product details
- Brand name
- Potassium Chloride
- Generic name
- Potassium Chloride
- Labeler
- Strides Pharma Science Limited
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210733
- Marketed since
- November 27, 2018
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 64380-861-06 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-861-06) | Nov 27, 2018 |
| 64380-861-07 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-861-07) | Nov 27, 2018 |
| 64380-861-08 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-861-08) | Nov 27, 2018 |
Recalls mentioning this NDC
- D-0006-2022 Oct 20, 2021 · Class II
Failed Dissolution Specifications - D-0001-2021 Oct 7, 2020 · Class II
Failed Dissolution Specifications - D-1029-2020 Mar 25, 2020 · Class III
Failed Tablet/Capsules Specifications: Oversized tablets were found in one lot of Potassium Chloride Tablets 750 mg.
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