NDC 61919-836
Alprazolam 1 mg tablet
On the label: Direct Rx. It's repackaged from NDC 67253-902, made by Par Pharmaceutical (Alprazolam). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). 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 Direct Rx names for other drugs.
Recalls
- Mar 4, 2022 · Class II · Direct Rx
CGMP Deviations: The Recall is due to the potential cross-contamination at the contract manufacturer (Ultra Tab Laboratories Inc.)
Lots: Lot #: 19AU1910 Exp. 5/31/22
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Alprazolam: every company that makes it
- Form
- tablet
- Strength
- 1 mg
- Approval
- ANDA ANDA074174
- On the market since
- Jul 12, 2019
- Package NDCs
61919-836-6061919-836-90- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?