NDC 61919-452
Hydrocodone Bitartrate And Acetaminophen 325 mg / 7.5 mg tablet
On the label: Direct Rx. It's repackaged from NDC 51862-586, made by Mayne Pharma Inc. (Lorcet Plus). 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.
Product details
- Generic drug
- Acetaminophen and Hydrocodone: every company that makes it
- Form
- tablet
- Strength
- 325 mg / 7.5 mg
- Approval
- ANDA ANDA090118
- On the market since
- Jul 22, 2019
- Package NDCs
61919-452-30- Official label
- DailyMed (National Library of Medicine), updated Jul 22, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?