NDC 72888-162 – Tramadol Hydrochloride

Tramadol Hydrochloride 25 mg/1 · Tablet, Coated · Oral

Human Prescription Drug DEA schedule CIV 1 recall

Product NDC72888-162

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Advagen Pharma Limited
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208708
Marketed since
November 28, 2023
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
72888-162-001000 TABLET, COATED in 1 BOTTLE (72888-162-00)Nov 28, 2023
72888-162-01100 TABLET, COATED in 1 BOTTLE (72888-162-01)Nov 28, 2023
72888-162-05500 TABLET, COATED in 1 BOTTLE (72888-162-05)Nov 28, 2023
72888-162-3030 TABLET, COATED in 1 BOTTLE (72888-162-30)Nov 28, 2023

Recalls mentioning this NDC

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