NDC 54868-3799
Prempro 2.5 mg / 0.625 mg tablet, sugar coated
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 0046-0875, made by Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc. (Prempro). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that relabels it). 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 Physicians Total Care, Inc. names for other drugs.
Product details
- Generic drug
- Estrogens, Conjugated and Medroxyprogesterone: every company that makes it
- Form
- tablet, sugar coated
- Strength
- 2.5 mg / 0.625 mg
- Approval
- NDA NDA020527
- On the market since
- Jun 20, 1996
- Package NDCs
54868-3799-0- Official label
- DailyMed (National Library of Medicine), updated Nov 1, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?