Propranolol Hydrochloride 00378-0185
Product NDC
00378-0185- Manufacturer
- Mylan Pharmaceuticals Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 19, 1985
- Listing Expires
- December 31, 2027
- Application
- ANDA070213
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Propranolol Hydrochloride | 80 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE, PLASTIC (0378-0185-01)
500 TABLET in 1 BOTTLE, PLASTIC (0378-0185-05)