NDC 71335-3147 – Tramadol Hydrochloride

Tramadol Hydrochloride 50 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-3147

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075968
Marketed since
August 5, 2024
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-3147-050 TABLET in 1 BOTTLE (71335-3147-0)Jun 18, 2026
71335-3147-130 TABLET in 1 BOTTLE (71335-3147-1)Jun 18, 2026
71335-3147-220 TABLET in 1 BOTTLE (71335-3147-2)Jun 18, 2026
71335-3147-390 TABLET in 1 BOTTLE (71335-3147-3)Jun 18, 2026
71335-3147-460 TABLET in 1 BOTTLE (71335-3147-4)Jun 18, 2026
71335-3147-5120 TABLET in 1 BOTTLE (71335-3147-5)Jun 18, 2026
71335-3147-6180 TABLET in 1 BOTTLE (71335-3147-6)Jun 18, 2026
71335-3147-740 TABLET in 1 BOTTLE (71335-3147-7)Jun 18, 2026
71335-3147-8100 TABLET in 1 BOTTLE (71335-3147-8)Jun 18, 2026
71335-3147-915 TABLET in 1 BOTTLE (71335-3147-9)Jun 18, 2026

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