NDC 68788-8121 – Tramadol Hydrochloride

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

Human Prescription Drug DEA schedule CIV

Product NDC68788-8121

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208708
Marketed since
January 5, 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
68788-8121-1100 TABLET, COATED in 1 BOTTLE (68788-8121-1)Jan 5, 2022
68788-8121-220 TABLET, COATED in 1 BOTTLE (68788-8121-2)Jan 5, 2022
68788-8121-330 TABLET, COATED in 1 BOTTLE (68788-8121-3)Jan 5, 2022
68788-8121-440 TABLET, COATED in 1 BOTTLE (68788-8121-4)Jan 5, 2022
68788-8121-515 TABLET, COATED in 1 BOTTLE (68788-8121-5)Jan 5, 2022
68788-8121-660 TABLET, COATED in 1 BOTTLE (68788-8121-6)Jan 5, 2022
68788-8121-750 TABLET, COATED in 1 BOTTLE (68788-8121-7)Jan 5, 2022
68788-8121-8120 TABLET, COATED in 1 BOTTLE (68788-8121-8)Jan 5, 2022
68788-8121-990 TABLET, COATED in 1 BOTTLE (68788-8121-9)Jan 5, 2022

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