NDC 71335-1676 – Tramadol Hydrochloride

Tramadol Hydrochloride 200 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-1676

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA201384
Marketed since
December 12, 2011
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
71335-1676-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-1)Jul 10, 2020
71335-1676-260 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-2)Jul 8, 2020
71335-1676-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-3)Aug 13, 2020
71335-1676-4120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-4)Apr 4, 2024

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