NDC 51224-206 – Naltrexone Hydrochloride
Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC51224-206
Product details
- Brand name
- Naltrexone Hydrochloride
- Generic name
- Naltrexone Hydrochloride
- Labeler
- TAGI Pharma Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075274
- Marketed since
- September 23, 2013
- Marketing end
- November 30, 2027
- Pharmacologic class
- Opioid Antagonist
Active ingredients
- Naltrexone Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Naltrexone Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51224-206-30 | 30 TABLET, FILM COATED in 1 BOTTLE (51224-206-30) | Sep 23, 2013 |
| 51224-206-50 | 100 TABLET, FILM COATED in 1 BOTTLE (51224-206-50) | Sep 23, 2013 |
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