NDC 71205-685
Nortrel 7/7/7(28 Day Regimen) 6 ingredients kit
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0555-9012.
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · relabels it
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 #: 100040731, 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
- 6 ingredients
- Approval
- ANDA ANDA075478
- On the market since
- Jan 2, 2003
- Package NDCs
71205-685-28- Official label
- DailyMed (National Library of Medicine), updated Aug 1, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?