NDC 0115-1233 – Oxymorphone hydrochloride
Oxymorphone Hydrochloride 20 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC0115-1233
Product details
- Brand name
- Oxymorphone hydrochloride
- Generic name
- Oxymorphone hydrochloride
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079087
- Marketed since
- January 2, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Opioid Agonist
Active ingredients
- Oxymorphone Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Oxymorphone Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 0115-1233-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1233-01) | Jan 2, 2013 |
| 0115-1233-03 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1233-03) | Jan 2, 2013 |
| 0115-1233-08 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1233-08) | Jan 2, 2013 |
| 0115-1233-13 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1233-13) | Jan 2, 2013 |
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- 0115-1316 Oxymorphone Hydrochloride 15 mg/1 · Tablet, Film Coated, Extended Release · Amneal Pharmaceuticals of New York LLC
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