NDC 68788-8717 – Tramadol hydrochloride

Tramadol Hydrochloride 50 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC68788-8717

Product details

Brand name
Tramadol hydrochloride
Generic name
Tramadol hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202075
Marketed since
July 18, 2024
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
68788-8717-1100 TABLET in 1 BOTTLE (68788-8717-1)Jul 18, 2024
68788-8717-220 TABLET in 1 BOTTLE (68788-8717-2)Jul 18, 2024
68788-8717-330 TABLET in 1 BOTTLE (68788-8717-3)Jul 18, 2024
68788-8717-440 TABLET in 1 BOTTLE (68788-8717-4)Jul 18, 2024
68788-8717-515 TABLET in 1 BOTTLE (68788-8717-5)Jul 18, 2024
68788-8717-660 TABLET in 1 BOTTLE (68788-8717-6)Jul 18, 2024
68788-8717-750 TABLET in 1 BOTTLE (68788-8717-7)Jul 18, 2024
68788-8717-8120 TABLET in 1 BOTTLE (68788-8717-8)Jul 18, 2024
68788-8717-990 TABLET in 1 BOTTLE (68788-8717-9)Jul 18, 2024

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