NDC 0406-0522 – Oxycodone And Acetaminophen
Oxycodone Hydrochloride 7.5 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral
Product NDC0406-0522
Product details
- Brand name
- Oxycodone And Acetaminophen
- Generic name
- Oxycodone hydrochloride and acetaminophen
- Labeler
- SpecGx LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040545
- Marketed since
- June 30, 2004
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 7.5 mg/1
- Acetaminophen 325 mg/1
Uses, dosage, side effects and warnings for Oxycodone And Acetaminophen →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 0406-0522-01 | 100 TABLET in 1 BOTTLE (0406-0522-01) | Jun 30, 2004 |
| 0406-0522-05 | 500 TABLET in 1 BOTTLE (0406-0522-05) | Jun 30, 2004 |
| 0406-0522-23 | 1 TABLET in 1 BLISTER PACK (0406-0522-23) | Jun 30, 2004 |
| 0406-0522-62 | 100 TABLET in 1 BLISTER PACK (0406-0522-62) | Jun 30, 2004 |
Recalls mentioning this NDC
- D-0255-2026 Jan 14, 2026 · Class II
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets. - D-0254-2026 Jan 14, 2026 · Class II
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
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