NDC 16571-782 – Cyclobenzaprine Hydrochloride

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

Human Prescription Drug

Product NDC16571-782

Product details

Brand name
Cyclobenzaprine Hydrochloride
Generic name
Cyclobenzaprine Hydrochloride
Labeler
Rising Pharma Holdings, Inc.
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
16571-782-01100 TABLET, FILM COATED in 1 BOTTLE (16571-782-01)Sep 26, 2008
16571-782-101000 TABLET, FILM COATED in 1 BOTTLE (16571-782-10)Sep 26, 2008
16571-782-50500 TABLET, FILM COATED in 1 BOTTLE (16571-782-50)Sep 26, 2008

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