Doxycycline Hyclate 70436-0201
Product NDC
70436-0201- Manufacturer
- Slate Run Pharmaceuticals, Llc
- Dosage Form
- Powder, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 22, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA217685
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Doxycycline Anhydrous | 200 mg/20mL |
Drug Class
Tetracycline-class Drug [EPC]Tetracycline-class Drug [EPC]Tetracyclines [CS]
Packaging Options(1)
10 VIAL, SINGLE-DOSE in 1 CARTON (70436-201-82) / 20 mL in 1 VIAL, SINGLE-DOSE (70436-201-36)