NDC 63187-981
Irbesartan and Hydrochlorothiazide 150 mg / 12.5 mg tablet, film coated
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-8238.
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 · repackages it and relabels it
Recalls
- Oct 20, 2015 · Class III · Teva Pharmaceutical Industries
Labeling: Incorrect or Missing Lot AND/OR Exp Date.
Lots: Lot #: 24I030, Exp 5/2017
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Hydrochlorothiazide and Irbesartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 150 mg / 12.5 mg
- Approval
- ANDA ANDA077369
- On the market since
- Jan 24, 2013
- Package NDCs
63187-981-3063187-981-6063187-981-90- Official label
- DailyMed (National Library of Medicine), updated Nov 1, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?