NDC 50090-0870
Truvada 200 mg / 300 mg tablet, film coated
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions 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
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels 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
50090-0870-050090-0870-250090-0870-3- Official label
- DailyMed (National Library of Medicine), updated Jun 15, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?