NDC 10702-055
Hydrocodone Bitartrate and Homatropine Methylbromide 5 mg / 1.5 mg tablet
On the label: KVK-TECH, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Kvk-Tech, Inc. | Newtown, PA, United States | Makes it | Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action |
Recalls
- Apr 27, 2021 · Class III · KVK-Tech, Inc.
Failed Impurities/Degradation Specifications
Lots: Lot: 15684A, Exp 7/2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Hydrocodone and Methylhomatropine: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg / 1.5 mg
- Approval
- ANDA ANDA207176
- On the market since
- Aug 7, 2017
- Package NDCs
10702-055-0110702-055-0310702-055-0910702-055-10- Official label
- DailyMed (National Library of Medicine), updated Aug 25, 2026
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