NDC 69238-2348 – Tramadol Hydrochloride

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

Human Prescription Drug DEA schedule CIV

Product NDC69238-2348

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA076003
Marketed since
November 15, 2010
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
69238-2348-1100 TABLET, COATED in 1 BOTTLE (69238-2348-1)Nov 15, 2010
69238-2348-410 TABLET, COATED in 1 BOTTLE (69238-2348-4)Nov 15, 2010
69238-2348-5500 TABLET, COATED in 1 BOTTLE (69238-2348-5)Nov 15, 2010
69238-2348-71000 TABLET, COATED in 1 BOTTLE (69238-2348-7)Nov 15, 2010

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