NDC 21695-595
Neomycin and Polymyxin B Sulfates and Dexamethasone 1 mg per 1 mL / 3.5 mg per 1 mL / 10000 mg per 1 mL suspension
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Sandoz Inc.'s NDC 61314-630.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Sandoz Inc. names for other drugs.
Recalls
- Oct 17, 2019 · Class III · Sandoz Inc
Labeling: Incorrect or missing package insert.
Lots: Lot #s: 287880F, 287881F, Exp. 10/31/2019; 290555F, Exp. 11/30/2019; 293389F, Exp. 2/29/2020; 290556F, 290557F, 293386F, 293387F, Exp. 3/31/2020; 293388F, 293390F, Exp. 5/31/2020; 293391F, Exp. 6/30/2020; 293392F, Exp. 7/31/2020; 295342F, 298823F, Exp. 8/31/2020; 295344F, 295345F, 295346F, Exp. 10/…
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Dexamethasone and Neomycin and Polymyxin B: every company that makes it
- Form
- suspension
- Strength
- 1 mg per 1 mL / 3.5 mg per 1 mL / 10000 mg per 1 mL
- Approval
- ANDA ANDA062721
- On the market since
- Nov 17, 1986
- Package NDCs
21695-595-05- Official label
- DailyMed (National Library of Medicine), updated Oct 8, 2010
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