NDC 71335-0082 – Propranolol Hydrochloride
Propranolol Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC71335-0082
Product details
- Brand name
- Propranolol Hydrochloride
- Generic name
- Propranolol hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA070221
- Marketed since
- June 21, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Propranolol Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Propranolol Hydrochloride →
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0082-1 | 20 TABLET in 1 BOTTLE (71335-0082-1) | Jan 18, 2013 |
| 71335-0082-2 | 30 TABLET in 1 BOTTLE (71335-0082-2) | Jan 18, 2013 |
| 71335-0082-3 | 100 TABLET in 1 BOTTLE (71335-0082-3) | Jan 18, 2013 |
| 71335-0082-4 | 60 TABLET in 1 BOTTLE (71335-0082-4) | Jan 18, 2013 |
| 71335-0082-5 | 90 TABLET in 1 BOTTLE (71335-0082-5) | Jan 18, 2013 |
| 71335-0082-6 | 180 TABLET in 1 BOTTLE (71335-0082-6) | Jan 18, 2013 |
| 71335-0082-7 | 28 TABLET in 1 BOTTLE (71335-0082-7) | Dec 31, 2015 |
| 71335-0082-8 | 10 TABLET in 1 BOTTLE (71335-0082-8) | Dec 31, 2015 |
| 71335-0082-9 | 120 TABLET in 1 BOTTLE (71335-0082-9) | Dec 31, 2015 |
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