NDC 67296-1502
Sulfamethoxazole and Trimethoprim 40 mg per 5 mL / 200 mg per 5 mL suspension
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Akorn's NDC 50383-824.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Akorn | Location not on file | Makes it and packages it | Not inspected on record |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Recalls
- Mar 13, 2017 · Class II · Akorn Inc
Failed Dissolution Specifications
Lots: Lot# 348913, Exp.01/18; Lot# 349552, Exp.03/18; Lot# 349681, Exp. 03/18; Lot# 349683, Exp. 03/18; Lot# 349685, Exp. 03/18; Lot# 349687, Exp. 03/18; Lot# 349689, Exp. 03/18; Lot# 350636, Exp.03/18
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sulfamethoxazole and Trimethoprim: every company that makes it
- Form
- suspension
- Strength
- 40 mg per 5 mL / 200 mg per 5 mL
- Approval
- ANDA ANDA074650
- On the market since
- Dec 29, 1997
- Package NDCs
67296-1502-167296-1502-2- Official label
- DailyMed (National Library of Medicine), updated Aug 1, 2024
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