NDC 80425-0548 – Tramadol Hydrochloride

Tramadol Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC80425-0548

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211825
Marketed since
August 27, 2025
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
80425-0548-115 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-1)Aug 27, 2025
80425-0548-230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-2)Aug 27, 2025
80425-0548-360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-3)Aug 27, 2025
80425-0548-490 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-4)Aug 27, 2025
80425-0548-5120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-5)Aug 27, 2025
80425-0548-640 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-6)Aug 27, 2025
80425-0548-7180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-7)Aug 27, 2025
80425-0548-8240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-8)Aug 27, 2025

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