Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 27808-0086-02 recalled?

Hydrocodone Polistirex and Chlorpheniramine Polistirex extended-release · 473 mL in 1 BOTTLE (27808-086-02)

Yes — this exact package was recalled

1 FDA recall names the code 27808-0086-02 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Hydrocodone Polistirex and Chlorpheniramine Polistirex
Strength
HYDROCODONE BITARTRATE 10 mg/5mL; CHLORPHENIRAMINE MALEATE…
Form
Suspension, Extended Release · Oral
Labeler
Cranbury Pharmaceuticals, LLC
Type
Human Prescription Drug · DEA CII
Product code
27808-0086

Recalls naming this package

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler