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Tramadol Hydrochloride

NDC 72888-162 · Advagen Pharma Limited

Generic nameTramadol Hydrochloride
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)TRAMADOL HYDROCHLORIDE
Strength25 mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCIV
Marketing categoryANDA

Packages

72888-162-00 — 1000 TABLET, COATED in 1 BOTTLE (72888-162-00)

72888-162-01 — 100 TABLET, COATED in 1 BOTTLE (72888-162-01)

72888-162-05 — 500 TABLET, COATED in 1 BOTTLE (72888-162-05)

72888-162-30 — 30 TABLET, COATED in 1 BOTTLE (72888-162-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71610-006 — Tramadol Hydrochloride, 71610-865 — Tramadol Hydrochloride, 72162-2510 — Tramadol Hydrochloride and Acetaminophen, 72189-154 — TRAMADOL HYDROCHLORIDE, 72189-311 — TRAMADOL HYDROCHLORIDE, 72189-382 — Tramadol Hydrochloride and Acetaminophen, 72189-521 — Tramadol HCL ER, 72189-671 — Tramadol/APAP, 72888-008 — Tramadol Hydrochloride, 72888-080 — Tramadol Hydrochloride, 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, +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 August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.