Propranolol Hydrochloride 60687-0609
Product NDC
60687-0609- Manufacturer
- American Health Packaging
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 9, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA070322
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Propranolol Hydrochloride | 40 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(1)
100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-609-01) / 1 TABLET in 1 BLISTER PACK (60687-609-11)