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Tramadol Hydrochloride

NDC 76420-734 · Asclemed USA, Inc.

Generic nameTramadol Hydrochloride
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)TRAMADOL HYDROCHLORIDE
Strength100 mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCIV
Marketing categoryANDA

Packages

76420-734-00 — 1000 TABLET, COATED in 1 BOTTLE (76420-734-00)

76420-734-01 — 100 TABLET, COATED in 1 BOTTLE (76420-734-01)

76420-734-05 — 500 TABLET, COATED in 1 BOTTLE (76420-734-05)

76420-734-30 — 30 TABLET, COATED in 1 BOTTLE (76420-734-30)

76420-734-60 — 60 TABLET, COATED in 1 BOTTLE (76420-734-60)

76420-734-90 — 90 TABLET, COATED in 1 BOTTLE (76420-734-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72888-163 — Tramadol Hydrochloride, 76420-105 — TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN, 76420-244 — TRAMADOL HYDROCHLORIDE, 76420-245 — TRAMADOL HYDROCHLORIDE, 76420-246 — TRAMADOL HYDROCHLORIDE, 76420-536 — TRAMADOL HYDROCHLORIDE, 76420-537 — TRAMADOL HYDROCHLORIDE, 76420-538 — TRAMADOL HYDROCHLORIDE, 76420-732 — Tramadol Hydrochloride, 76420-733 — Tramadol Hydrochloride, 76420-983 — Tramadol Hydrochloride and Acetaminophen, 80425-0057 — Tramadol HCL, 80425-0108 — Tramadol HCL, 80425-0127 — Tramadol HCL, 80425-0136 — Tramadol HCL, 80425-0141 — Tramadol HCL, 80425-0274 — Tramadol Hydrochloride, 80425-0276 — Tramadol Hydrochloride, 80425-0312 — Tramadol HCL, 80425-0501 — Tramadol Hydrochloride, +120 more

Poisoning, adverse-effect and underdosing codes for this drug

The ICD-10-CM Table of Drugs and Chemicals carries these diagnosis codes for this drug — a drug-name match derived from FDA's product name and the Table of Drugs and Chemicals, not a CMS-published pairing.

T40.421 — Poisoning by tramadol, accidental (unintentional), T40.422 — Poisoning by tramadol, intentional self-harm, T40.423 — Poisoning by tramadol, assault, T40.424 — Poisoning by tramadol, undetermined, T40.425 — Adverse effect of tramadol, T40.426 — Underdosing of tramadol

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.