NDC 17856-0457
Polyethylene Glycol 3350 17 g per 17 g powder, for solution
On the label: Atlantic Biologicals Corps.. It's repackaged from NDC 51991-457, made by Breckenridge Pharmaceutical, Inc. (Polyethylene Glycol 3350). 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 repackages it and 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 Atlantic Biologicals Corps. names for other drugs.
Product details
- Generic drug
- Polyethylene Glycol 3350: every company that makes it
- Form
- powder, for solution
- Strength
- 17 g per 17 g
- Approval
- ANDA ANDA077706
- On the market since
- Sep 6, 2006
- Package NDCs
17856-0457-117856-0457-217856-0457-317856-0457-417856-0457-517856-0457-6- Official label
- DailyMed (National Library of Medicine), updated May 22, 2018
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