NDC 65862-190 – Cyclobenzaprine Hydrochloride

Cyclobenzaprine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65862-190

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078643
Marketed since
September 26, 2008
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
65862-190-01100 TABLET, FILM COATED in 1 BOTTLE (65862-190-01)Sep 26, 2008
65862-190-05500 TABLET, FILM COATED in 1 BOTTLE (65862-190-05)Sep 26, 2008
65862-190-991000 TABLET, FILM COATED in 1 BOTTLE (65862-190-99)Sep 26, 2008

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