NDC 76420-537 – Tramadol Hydrochloride

Tramadol Hydrochloride 200 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CIV

Product NDC76420-537

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA200503
Marketed since
August 19, 2014
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
76420-537-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-537-30)Feb 16, 2023
76420-537-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-537-60)Feb 16, 2023
76420-537-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-537-90)Feb 16, 2023

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