NDC 61314-238 – Carteolol Hydrochloride
Carteolol Hydrochloride 10 mg/mL · Solution · Ophthalmic
Product NDC61314-238
Product details
- Brand name
- Carteolol Hydrochloride
- Generic name
- Carteolol Hydrochloride
- Labeler
- Sandoz Inc
- Dosage form
- Solution
- Route
- Ophthalmic
- Marketing category
- ANDA · ANDA075476
- Marketed since
- January 5, 2000
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Carteolol Hydrochloride 10 mg/mL
Uses, dosage, side effects and warnings for Carteolol Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 61314-238-05 | 5 mL in 1 BOTTLE, PLASTIC (61314-238-05) | Jan 5, 2000 |
| 61314-238-10 | 10 mL in 1 BOTTLE, PLASTIC (61314-238-10) | Jan 5, 2000 |
| 61314-238-15 | 15 mL in 1 BOTTLE, PLASTIC (61314-238-15) | Jan 5, 2000 |