NDC 70518-2031
Buspirone Hydrochloride 10 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-024.
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 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. names for other drugs.
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA204582
- On the market since
- Apr 18, 2019
- Package NDCs
70518-2031-070518-2031-170518-2031-270518-2031-370518-2031-470518-2031-5- Official label
- DailyMed (National Library of Medicine), updated Jul 16, 2026
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