NDC 10702-150
Hydrocodone Bitartrate and Homatropine Methylbromide 5 mg per 5 mL / 1.5 mg per 5 mL liquid
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
- Nov 1, 2019 · Class II · KVK-Tech, Inc.
Presence of Foreign Substance: Black particles were found in the lots during retain sample inspection
Lots: Lot #: 14375A, Exp. date 2019-DEC; 14398A, Exp. date 2020-JAN
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
- liquid, oral
- Strength
- 5 mg per 5 mL / 1.5 mg per 5 mL
- Approval
- ANDA ANDA207487
- On the market since
- Feb 21, 2017
- Package NDCs
10702-150-16- Official label
- DailyMed (National Library of Medicine), updated May 22, 2026
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