NDC 71335-2518 – Tramadol hydrochloride

Tramadol Hydrochloride 50 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-2518

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, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-2518-050 TABLET in 1 BOTTLE (71335-2518-0)Nov 4, 2024
71335-2518-130 TABLET in 1 BOTTLE (71335-2518-1)Nov 4, 2024
71335-2518-220 TABLET in 1 BOTTLE (71335-2518-2)Nov 4, 2024
71335-2518-390 TABLET in 1 BOTTLE (71335-2518-3)Nov 4, 2024
71335-2518-460 TABLET in 1 BOTTLE (71335-2518-4)Nov 4, 2024
71335-2518-5120 TABLET in 1 BOTTLE (71335-2518-5)Nov 4, 2024
71335-2518-6180 TABLET in 1 BOTTLE (71335-2518-6)Nov 4, 2024
71335-2518-740 TABLET in 1 BOTTLE (71335-2518-7)Nov 4, 2024
71335-2518-8100 TABLET in 1 BOTTLE (71335-2518-8)Nov 4, 2024
71335-2518-915 TABLET in 1 BOTTLE (71335-2518-9)Nov 4, 2024

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