NDC 49502-476

Pretomanid 200 mg tablet

On the label: Viatris Specialty LLC.

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 Viatris Specialty LLC names for other drugs.

Product details

Generic drug: Pretomanid: every company that makes it
Form: tablet, oral
Strength: 200 mg
Approval: NDA NDA212862
On the market since: Nov 7, 2019
Package NDCs: 49502-476-14 49502-476-26 49502-476-29 49502-476-32 49502-476-33 49502-476-72
Official label: DailyMed (National Library of Medicine), updated Nov 15, 2024

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