Where it's 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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Recalls
- Mar 14, 2013 · Class III · Teva Pharmaceuticals USA, Inc.
Failed Impurity/Degradation Specifications; an impurity identified as N-Butyl-Benzene Sulfonamide (NBBS) detected during impurity testing
Lots: NDC 0555-3134-82 and 0093-3134-91 -- lot numbers 33802566A, exp 3/2013; 33802967A, exp 8/2013; 33803529A, exp 10/2013; and 33803609A, exp 11/2013.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ethinyl Estradiol and Levonorgestrel: every company that makes it
- Form
- kit
- Strength
- 0.01 mg / 0.03 mg / 0.15 mg
- Approval
- NDA authorized generic NDA021840
- On the market since
- Jul 28, 2011
- Package NDCs
0093-3134-820093-3134-91- Official label
- DailyMed (National Library of Medicine), updated Oct 31, 2024
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