NDC 67296-1237
Truvada 200 mg / 300 mg tablet, film coated
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Gilead Sciences, Inc.'s NDC 61958-0701.
Where the pills inside were 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 Gilead Sciences, Inc. names for other drugs.
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Recalls
- Sep 30, 2014 · Class III · Gilead Sciences, Inc.
Presence of Foreign Substance: Truvada was found to contain small red silicone rubber particulates.
Lots: TRUVADA (NDA 21-752; NDC 61958-0701-1) Lot# 002808, Expiration Date: 31 December 2017
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Emtricitabine and Tenofovir: every company that makes it
- Form
- tablet, film coated
- Strength
- 200 mg / 300 mg
- Approval
- NDA NDA021752
- On the market since
- Aug 2, 2004
- Package NDCs
67296-1237-367296-1237-4- Official label
- DailyMed (National Library of Medicine), updated Jul 15, 2024
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