NDC 42254-006
Betadine 5 mg per 1 mL solution
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Alcon Laboratories, Inc.'s NDC 0065-0411.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Woodstock Sterile Solutions, Inc. | Woodstock, IL, United States | Makes it | No problems foundOct 13, 2022 · 11 inspections |
Recalls
- Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Iodine: every company that makes it
- Form
- solution
- Strength
- 5 mg per 1 mL
- Approval
- NDA NDA018634
- On the market since
- Apr 1, 2000
- Package NDCs
42254-006-30- Official label
- DailyMed (National Library of Medicine), updated Oct 25, 2011
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?