NDC 64950-354 – Oxycodone Hydrochloride
Oxycodone Hydrochloride 5 mg/5mL · Solution · Oral
Product NDC64950-354
Product details
- Brand name
- Oxycodone Hydrochloride
- Generic name
- Oxycodone Hydrochloride
- Labeler
- Genus Lifesciences Inc.
- Dosage form
- Solution
- Route
- Oral
- Marketing category
- NDA · NDA200535
- Marketed since
- September 9, 2013
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 5 mg/5mL
Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 64950-354-10 | 1 BOTTLE, PLASTIC in 1 CARTON (64950-354-10) / 100 mL in 1 BOTTLE, PLASTIC | Sep 9, 2013 |
| 64950-354-45 | 40 CUP, UNIT-DOSE in 1 CASE (64950-354-45) / 5 mL in 1 CUP, UNIT-DOSE (64950-354-05) | Sep 9, 2013 |
| 64950-354-50 | 1 BOTTLE, PLASTIC in 1 CARTON (64950-354-50) / 500 mL in 1 BOTTLE, PLASTIC | Sep 9, 2013 |
| 64950-354-55 | 50 CUP, UNIT-DOSE in 1 CASE (64950-354-55) / 5 mL in 1 CUP, UNIT-DOSE (64950-354-05) | Sep 9, 2013 |
Recalls mentioning this NDC
- D-0231-2021 Jan 20, 2021 · Class III
Presence of Foreign Substance: Particulate matter was found in multiple lots of product.
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