NDC 68788-4035 – Tramadol Hydrochloride

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

Human Prescription Drug DEA schedule CIV

Product NDC68788-4035

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
September 29, 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
68788-4035-1100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-1)Sep 29, 2025
68788-4035-220 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-2)Sep 29, 2025
68788-4035-330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-3)Sep 29, 2025
68788-4035-440 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-4)Sep 29, 2025
68788-4035-515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-5)Sep 29, 2025
68788-4035-660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-6)Sep 29, 2025
68788-4035-760 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-7)Sep 29, 2025
68788-4035-8120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-8)Sep 29, 2025
68788-4035-990 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-9)Sep 29, 2025

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