Carteolol Hydrochloride 61314-0238
Product NDC
61314-0238- Manufacturer
- Sandoz Inc
- Dosage Form
- Solution
- Route
- Ophthalmic
- Product Type
- Human Prescription Drug
- Marketing Start
- January 5, 2000
- Listing Expires
- December 31, 2026
- Application
- ANDA075476
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Carteolol Hydrochloride | 10 mg/mL |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(3)
5 mL in 1 BOTTLE, PLASTIC (61314-238-05)
10 mL in 1 BOTTLE, PLASTIC (61314-238-10)
15 mL in 1 BOTTLE, PLASTIC (61314-238-15)