NDC 71335-9670 – Tramadol Hydrochloride

Tramadol Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-9670

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA200503
Marketed since
August 19, 2014
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
71335-9670-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9670-1)Mar 24, 2023
71335-9670-260 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9670-2)Apr 13, 2026
71335-9670-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9670-3)Jan 6, 2026
71335-9670-4120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9670-4)Apr 13, 2026

Other Tramadol Hydrochloride products