Sodium Phosphates 68462-0729
Product NDC
68462-0729- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- February 23, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA220683
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sodium Phosphate, Dibasic, Heptahydrate | 268 mg/mL |
| Sodium Phosphate, Monobasic, Monohydrate | 276 mg/mL |
Packaging Options(1)
25 VIAL, SINGLE-DOSE in 1 CARTON (68462-729-25) / 15 mL in 1 VIAL, SINGLE-DOSE (68462-729-15)