NDC 27808-301 – Tramadol Hydrochloride

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

Human Prescription Drug DEA schedule CIV

Product NDC27808-301

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Cranbury Pharmaceuticals, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091498
Marketed since
December 22, 2024
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
27808-301-01100 TABLET, FILM COATED in 1 BOTTLE (27808-301-01)Dec 22, 2024
27808-301-02500 TABLET, FILM COATED in 1 BOTTLE (27808-301-02)Dec 22, 2024
27808-301-031000 TABLET, FILM COATED in 1 BOTTLE (27808-301-03)Dec 22, 2024

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