NDC 76420-733 – Tramadol Hydrochloride

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

Human Prescription Drug DEA schedule CIV

Product NDC76420-733

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208708
Marketed since
July 24, 2023
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
76420-733-001000 TABLET, COATED in 1 BOTTLE (76420-733-00)May 22, 2024
76420-733-01100 TABLET, COATED in 1 BOTTLE (76420-733-01)May 22, 2024
76420-733-022 TABLET, COATED in 1 BOTTLE (76420-733-02)Aug 14, 2025
76420-733-05500 TABLET, COATED in 1 BOTTLE (76420-733-05)May 22, 2024
76420-733-101 TABLET, COATED in 1 BOTTLE (76420-733-10)Aug 14, 2025
76420-733-12120 TABLET, COATED in 1 BOTTLE (76420-733-12)Jul 14, 2025
76420-733-3030 TABLET, COATED in 1 BOTTLE (76420-733-30)May 22, 2024
76420-733-6060 TABLET, COATED in 1 BOTTLE (76420-733-60)May 22, 2024
76420-733-9090 TABLET, COATED in 1 BOTTLE (76420-733-90)May 22, 2024

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