NDC 70518-4068
Buspirone Hydrochloride 30 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Unichem Pharmaceuticals (USA), Inc.'s NDC 29300-478.
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 Unichem Pharmaceuticals (USA), Inc. names for other drugs.
Recalls
- Apr 13, 2026 · Class III · Unichem Pharmaceuticals USA Inc.
Subpotent drug
Lots: Lot: ZBUL25001, Exp 12/31/2027
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA210907
- On the market since
- May 5, 2024
- Package NDCs
70518-4068-0- Official label
- DailyMed (National Library of Medicine), updated Aug 27, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?