NDC 54868-5385
Anagrelide Hydrochloride 1 mg capsule
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 0172-5240, made by Teva Pharmaceuticals USA, Inc. (Anagrelide Hydrochloride). 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. 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
- Anagrelide: every company that makes it
- Form
- capsule
- Strength
- 1 mg
- Approval
- ANDA ANDA076468
- On the market since
- Aug 15, 2005
- Package NDCs
54868-5385-054868-5385-1- Official label
- DailyMed (National Library of Medicine), updated Apr 27, 2012
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