NDC 59762-2135 – Amlodipine besylate

Amlodipine Besylate 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC59762-2135

Product details

Brand name
Amlodipine besylate
Generic name
Amlodipine besylate
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA019787
Marketed since
June 24, 2019
Listing expires
December 31, 2027
Pharmacologic class
Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Amlodipine besylate →

Package NDC codes (2)

Package NDCDescriptionSince
59762-2135-11000 TABLET in 1 BOTTLE (59762-2135-1)Nov 13, 2019
59762-2135-990 TABLET in 1 BOTTLE (59762-2135-9)Jun 24, 2019

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