NDC 70518-3466 – Propranolol Hydrochloride
Propranolol Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC70518-3466
Product details
- Brand name
- Propranolol Hydrochloride
- Generic name
- Propranolol Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA071972
- Marketed since
- August 3, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Propranolol Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Propranolol Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 70518-3466-2 | 30 TABLET in 1 BLISTER PACK (70518-3466-2) | Oct 24, 2022 |
| 70518-3466-3 | 30 TABLET in 1 BLISTER PACK (70518-3466-3) | Jan 31, 2024 |
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