NDC 69097-869 – Nadolol

Nadolol 80 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC69097-869

Product details

Brand name
Nadolol
Generic name
Nadolol
Labeler
Cipla USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203455
Marketed since
February 23, 2016
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nadolol →

Package NDC codes (3)

Package NDCDescriptionSince
69097-869-0230 TABLET in 1 BOTTLE (69097-869-02)Feb 23, 2016
69097-869-07100 TABLET in 1 BOTTLE (69097-869-07)Feb 23, 2016
69097-869-151000 TABLET in 1 BOTTLE (69097-869-15)Feb 23, 2016

Recalls mentioning this NDC

Other Nadolol products