NDC 27808-086 – Hydrocodone Polistirex and Chlorpheniramine Polistirex extended-release

Hydrocodone Bitartrate 10 mg/5mL; Chlorpheniramine Maleate 8 mg/5mL · Suspension, Extended Release · Oral

Human Prescription Drug DEA schedule CII 1 recall

Product NDC27808-086

Product details

Brand name
Hydrocodone Polistirex and Chlorpheniramine Polistirex extended-release
Generic name
Hydrocodone Polistirex and Chlorpheniramine Polistirex
Labeler
Cranbury Pharmaceuticals, LLC
Dosage form
Suspension, Extended Release
Route
Oral
Marketing category
ANDA · ANDA091632
Marketed since
March 6, 2015
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist; Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Hydrocodone Polistirex and Chlorpheniramine Polistirex →

Package NDC codes (2)

Package NDCDescriptionSince
27808-086-011 BOTTLE, UNIT-DOSE in 1 CARTON (27808-086-01) / 115 mL in 1 BOTTLE, UNIT-DOSEMar 6, 2015
27808-086-02473 mL in 1 BOTTLE (27808-086-02)Mar 6, 2015

Recalls mentioning this NDC

Other Hydrocodone Polistirex and Chlorpheniramine Polistirex products