NDC 71335-2612 – Tramadol hydrochloride

Tramadol Hydrochloride 50 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-2612

Product details

Brand name
Tramadol hydrochloride
Generic name
Tramadol hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202075
Marketed since
March 1, 2018
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
71335-2612-18 TABLET in 1 BOTTLE (71335-2612-1)Mar 11, 2026
71335-2612-284 TABLET in 1 BOTTLE (71335-2612-2)Mar 11, 2026
71335-2612-356 TABLET in 1 BOTTLE (71335-2612-3)Mar 11, 2026
71335-2612-410 TABLET in 1 BOTTLE (71335-2612-4)Mar 11, 2026

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