NDC 27808-086 – Hydrocodone Polistirex and Chlorpheniramine Polistirex extended-release
Hydrocodone Bitartrate 10 mg/5mL; Chlorpheniramine Maleate 8 mg/5mL · Suspension, Extended Release · Oral
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
- Hydrocodone Bitartrate 10 mg/5mL
- Chlorpheniramine Maleate 8 mg/5mL
Uses, dosage, side effects and warnings for Hydrocodone Polistirex and Chlorpheniramine Polistirex →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 27808-086-01 | 1 BOTTLE, UNIT-DOSE in 1 CARTON (27808-086-01) / 115 mL in 1 BOTTLE, UNIT-DOSE | Mar 6, 2015 |
| 27808-086-02 | 473 mL in 1 BOTTLE (27808-086-02) | Mar 6, 2015 |
Recalls mentioning this NDC
- D-1517-2019 Jul 31, 2019 · Class II
Superpotent Drug and Failed Stability Specifications: High out-of-specification results for the active ingredients, hydrocodone and chlorpheniramine, as well as high out-of-specification results for…
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