NDC 72189-311 – Tramadol Hydrochloride

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

Human Prescription Drug DEA schedule CIV

Product NDC72189-311

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
DirectRx
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208708
Marketed since
January 12, 2022
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
72189-311-1212 TABLET, COATED in 1 BOTTLE (72189-311-12)Jan 12, 2022
72189-311-2020 TABLET, COATED in 1 BOTTLE (72189-311-20)Jan 12, 2022
72189-311-3030 TABLET, COATED in 1 BOTTLE (72189-311-30)Jan 12, 2022
72189-311-4040 TABLET, COATED in 1 BOTTLE (72189-311-40)Jan 12, 2022
72189-311-6060 TABLET, COATED in 1 BOTTLE (72189-311-60)Jan 12, 2022
72189-311-72120 TABLET, COATED in 1 BOTTLE (72189-311-72)Jan 12, 2022
72189-311-82180 TABLET, COATED in 1 BOTTLE (72189-311-82)Jan 12, 2022
72189-311-84240 TABLET, COATED in 1 BOTTLE (72189-311-84)Jan 12, 2022
72189-311-9090 TABLET, COATED in 1 BOTTLE (72189-311-90)Jan 12, 2022

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