NDC 68788-4040 – Tramadol Hydrochloride

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

Human Prescription Drug DEA schedule CIV

Product NDC68788-4040

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211825
Marketed since
October 13, 2025
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
68788-4040-1100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-1)Oct 13, 2025
68788-4040-220 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-2)Oct 13, 2025
68788-4040-330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-3)Oct 13, 2025
68788-4040-440 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-4)Oct 13, 2025
68788-4040-515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-5)Oct 13, 2025
68788-4040-660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-6)Oct 13, 2025
68788-4040-750 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-7)Oct 13, 2025
68788-4040-8120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-8)Oct 13, 2025
68788-4040-990 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-9)Oct 13, 2025

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