NDC 0591-0795 – Dicyclomine Hydrochloride

Dicyclomine Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC0591-0795

Product details

Brand name
Dicyclomine Hydrochloride
Generic name
Dicyclomine Hydrochloride
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA085223
Marketed since
July 30, 1986
Listing expires
December 31, 2026
Pharmacologic class
Anticholinergic

Active ingredients

Uses, dosage, side effects and warnings for Dicyclomine Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
0591-0795-01100 TABLET in 1 BOTTLE, PLASTIC (0591-0795-01)Jul 30, 1986
0591-0795-101000 TABLET in 1 BOTTLE, PLASTIC (0591-0795-10)Jul 30, 1986

Recalls mentioning this NDC

Other Dicyclomine Hydrochloride products