NDC 68071-2695
Finasteride 5 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-525.
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 Camber Pharmaceuticals Inc. names for other drugs.
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Recalls
- Dec 29, 2016 · Class III · Hetero Drugs Ltd. - Unit 1
Failed Tablet/Capsule Specification: Tablets were found to be twice the thickness in one lot of product.
Lots: Lot #: FIN16002, Exp. 03/2018
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Finasteride: every company that makes it
- Form
- tablet, film coated
- Strength
- 5 mg
- Approval
- ANDA ANDA090061
- On the market since
- Jun 13, 2015
- Package NDCs
68071-2695-3- Official label
- DailyMed (National Library of Medicine), updated May 12, 2022
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?