NDC 80425-0588 – Tramadol Hydrochloride

Tramadol Hydrochloride 50 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC80425-0588

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075968
Marketed since
June 26, 2026
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
80425-0588-115 TABLET in 1 BOTTLE (80425-0588-1)Jun 26, 2026
80425-0588-230 TABLET in 1 BOTTLE (80425-0588-2)Jun 26, 2026
80425-0588-340 TABLET in 1 BOTTLE (80425-0588-3)Jun 26, 2026
80425-0588-460 TABLET in 1 BOTTLE (80425-0588-4)Jun 26, 2026
80425-0588-590 TABLET in 1 BOTTLE (80425-0588-5)Jun 26, 2026
80425-0588-6120 TABLET in 1 BOTTLE (80425-0588-6)Jun 26, 2026
80425-0588-7180 TABLET in 1 BOTTLE (80425-0588-7)Jun 26, 2026
80425-0588-8240 TABLET in 1 BOTTLE (80425-0588-8)Jun 26, 2026

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