NDC 0078-0364 – Lotrel
Amlodipine Besylate 10 mg/1; Benazepril Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC0078-0364
Product details
- Brand name
- Lotrel
- Generic name
- Amlodipine besylate and benazepril hydrochloride
- Labeler
- Novartis Pharmaceuticals Corporation
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- NDA · NDA020364
- Marketed since
- March 3, 1995
- Marketing end
- September 30, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Active ingredients
- Amlodipine Besylate 10 mg/1
- Benazepril Hydrochloride 20 mg/1
Package NDC codes (0)
| Package NDC | Description | Since |
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Other Lotrel products
- 0078-0379 Amlodipine Besylate 10 mg/1; Benazepril Hydrochloride 40 mg/1 · Capsule · Novartis Pharmaceuticals Corporation
- 0078-0405 Amlodipine Besylate 5 mg/1; Benazepril Hydrochloride 10 mg/1 · Capsule · Novartis Pharmaceuticals Corporation
- 0078-0406 Amlodipine Besylate 5 mg/1; Benazepril Hydrochloride 20 mg/1 · Capsule · Novartis Pharmaceuticals Corporation