NDC 17856-0604

Dextromethorphan Hydrobromide and Promethazine Hydrochloride 15 mg per 5 mL / 6.25 mg per 5 mL syrup

On the label: Atlantic Biologicals Corps.. It's repackaged from NDC 60432-604, made by Morton Grove Pharmaceuticals, Inc. (Promethazine Hydrochloride and Dextromethorphan Hydrobromide). 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). 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
Dextromethorphan and Promethazine: every company that makes it
Form
syrup
Strength
15 mg per 5 mL / 6.25 mg per 5 mL
Approval
ANDA ANDA088864
On the market since
Jan 4, 1985
Package NDCs
17856-0604-4 17856-0604-5
Official label
DailyMed (National Library of Medicine), updated Jun 5, 2024

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