NDC 67296-1642
Hydromorphone Hydrochloride 2 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged from NDC 0527-1353, made by Lannett Company, Inc. (Hydromorphone Hydrochloride). 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 and relabels 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 RedPharm Drug. Inc. names for other drugs.
Product details
- Generic drug
- Hydromorphone: every company that makes it
- Form
- tablet
- Strength
- 2 mg
- Approval
- ANDA ANDA077471
- On the market since
- Jan 1, 2019
- Package NDCs
67296-1642-9- Official label
- DailyMed (National Library of Medicine), updated Jan 14, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?