NDC 82619-135 – Propranolol Hydrochloride
Propranolol Hydrochloride 160 mg/1 · Capsule, Extended Release · Oral
Product NDC82619-135
Product details
- Brand name
- Propranolol Hydrochloride
- Generic name
- Propranolol Hydrochloride
- Labeler
- Creekwood Pharmaceuticals LLC
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA219460
- Marketed since
- August 29, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Propranolol Hydrochloride 160 mg/1
Uses, dosage, side effects and warnings for Propranolol Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 82619-135-01 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82619-135-01) | Aug 29, 2026 |
| 82619-135-02 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82619-135-02) | Aug 29, 2026 |
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