NDC 76420-366
Oxycodone Hydrochloride 30 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Strides Pharma Science Limited's NDC 64380-263.
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 Strides Pharma Science Limited names for other drugs.
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Oxycodone: every company that makes it
- Form
- tablet, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA077712
- On the market since
- Sep 10, 2024
- Package NDCs
76420-366-0176420-366-0576420-366-1076420-366-3076420-366-6076420-366-90- Official label
- DailyMed (National Library of Medicine), updated Dec 27, 2025
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