NDC 65862-861 – Darifenacin

Darifenacin Hydrobromide 7.5 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC65862-861

Product details

Brand name
Darifenacin
Generic name
Darifenacin
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA206743
Marketed since
September 19, 2016
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Muscarinic Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Darifenacin →

Package NDC codes (4)

Package NDCDescriptionSince
65862-861-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-861-05)Sep 19, 2016
65862-861-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-861-30)Sep 19, 2016
65862-861-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-861-90)Sep 19, 2016
65862-861-991000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-861-99)Sep 19, 2016

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