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 15, 2013 · Class III · Teva Pharmaceuticals USA, Inc.
Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Benzene Sulfonamide (NBBS) was detected during impurity testing
Lots: NDC 0555-9014-67, Lot numbers 33802921A, exp 8/2013; 33803173A, exp 10/2013; 33803695A, exp 2/2014; and 33803942A, exp 3/2014.
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
- 0.1 mg / 0.02 mg
- Approval
- ANDA ANDA075803
- On the market since
- Apr 22, 2002
- Package NDCs
0555-9014-670555-9014-79- Official label
- DailyMed (National Library of Medicine), updated Dec 16, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?