NDC 70518-3824 – Tramadol Hydrochloride

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

Human Prescription Drug DEA schedule CIV 1 recall

Product NDC70518-3824

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208708
Marketed since
August 7, 2023
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
70518-3824-030 TABLET, COATED in 1 BLISTER PACK (70518-3824-0)Aug 7, 2023
70518-3824-160 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-1)Aug 8, 2023
70518-3824-290 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-2)Aug 18, 2023
70518-3824-3180 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-3)Aug 18, 2023
70518-3824-4120 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-4)Aug 31, 2023
70518-3824-530 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-5)Oct 11, 2023
70518-3824-6100 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-6)Dec 18, 2025
70518-3824-7180 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-7)May 3, 2026
70518-3824-890 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-8)May 3, 2026
70518-3824-9180 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-9)Jun 14, 2026

Recalls mentioning this NDC

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