NDC 68180-150
Famotidine 40 mg per 5 mL powder, for suspension
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Recalls
- May 2, 2017 · Class III · Lupin Pharmaceuticals Inc.
CGMP Deviations
Lots: Lot #: G606950, Exp 07/18
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 40 mg per 5 mL
- Approval
- ANDA ANDA090440
- On the market since
- Jun 29, 2010
- Package NDCs
68180-150-01- Official label
- DailyMed (National Library of Medicine), updated Dec 29, 2025
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