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
- Jan 25, 2024 · Class III · Teva Pharmaceuticals USA, Inc
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
Lots: Lot #: 100042978, Exp 7/31/2024
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 Norethindrone: every company that makes it
- Form
- kit
- Strength
- 1 mg / 0.035 mg
- Approval
- ANDA ANDA072696
- On the market since
- Jun 6, 2001
- Package NDCs
0555-9010-580555-9010-79- Official label
- DailyMed (National Library of Medicine), updated Dec 1, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?