NDC 0406-1170 – Naltrexone Hydrochloride
Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC0406-1170
Product details
- Brand name
- Naltrexone Hydrochloride
- Generic name
- Naltrexone hydrochloride
- Labeler
- SpecGx LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076264
- Marketed since
- March 22, 2002
- Listing expires
- December 31, 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 |
|---|---|---|
| 0406-1170-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0406-1170-01) | Mar 22, 2002 |
| 0406-1170-03 | 30 TABLET, FILM COATED in 1 BOTTLE (0406-1170-03) | Mar 22, 2002 |
Recalls mentioning this NDC
- D-1039-2022 Jun 15, 2022 · Class II
cGMP deviations: Temperature abuse
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