NDC 0406-0512 – Oxycodone And Acetaminophen
Oxycodone Hydrochloride 5 mg/1; Acetaminophen 325 mg/1 · Tablet · Oral
Product NDC0406-0512
Product details
- Brand name
- Oxycodone And Acetaminophen
- Generic name
- oxycodone hydrochloride and acetaminophen
- Labeler
- SpecGx LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA087463
- Marketed since
- December 7, 1983
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxycodone Hydrochloride 5 mg/1
- Acetaminophen 325 mg/1
Uses, dosage, side effects and warnings for Oxycodone And Acetaminophen →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 0406-0512-01 | 100 TABLET in 1 BOTTLE (0406-0512-01) | Dec 7, 1983 |
| 0406-0512-05 | 500 TABLET in 1 BOTTLE (0406-0512-05) | Dec 7, 1983 |
| 0406-0512-23 | 1 TABLET in 1 BLISTER PACK (0406-0512-23) | Dec 7, 1983 |
| 0406-0512-62 | 100 TABLET in 1 BLISTER PACK (0406-0512-62) | Dec 7, 1983 |
| 0406-0512-91 | 5000 TABLET in 1 PAIL (0406-0512-91) | Dec 7, 1983 |
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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- 76420-136 Oxycodone Hydrochloride 5 mg/1; Acetaminophen 325 mg/1 · Tablet · Asclemed USA, Inc.
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