NDC 70771-1340 – Metoprolol succinate

Metoprolol Succinate 100 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC70771-1340

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA203894
Marketed since
June 7, 2018
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Metoprolol Succinate →

Package NDC codes (3)

Package NDCDescriptionSince
70771-1340-01000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1340-0)Jun 7, 2018
70771-1340-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1340-1)Jun 7, 2018
70771-1340-5500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1340-5)Jun 7, 2018

Other Metoprolol Succinate products