NDC 47335-861 – Tramadol Hydrochloride

Tramadol Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CIV

Product NDC47335-861

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA201384
Marketed since
December 12, 2011
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
47335-861-08100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-861-08)Dec 12, 2011
47335-861-181000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-861-18)Dec 12, 2011
47335-861-8330 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-861-83)Dec 12, 2011
47335-861-88100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-861-88)Dec 12, 2011

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