NDC 58160-815
Twinrix 20 ug per 1 mL / 720 [iU] per 1 mL injection, suspension
On the label: GlaxoSmithKline Biologicals SA.
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants GlaxoSmithKline Biologicals SA names for other drugs.
Product details
- Generic drug
- Hepatitis A Virus Strain Hm175 Antigen (formaldehyde Inactivated) and Hepatitis B Virus Subtype Adw2 Hbsag Surface Protein Antigen: every company that makes it
- Form
- injection, suspension, intramuscular
- Strength
- 20 ug per 1 mL / 720 [iU] per 1 mL
- Approval
- BLA BLA103850
- On the market since
- Jun 7, 2007
- Package NDCs
58160-815-4358160-815-52- Official label
- DailyMed (National Library of Medicine), updated May 14, 2026
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