NDC 16729-081 – Naltrexone Hydrochloride
Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC16729-081
Product details
- Brand name
- Naltrexone Hydrochloride
- Generic name
- Naltrexone Hydrochloride
- Labeler
- Accord Healthcare, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA091205
- Marketed since
- January 18, 2012
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 16729-081-01 | 100 TABLET, FILM COATED in 1 BOTTLE (16729-081-01) | Jan 18, 2012 |
| 16729-081-10 | 30 TABLET, FILM COATED in 1 BOTTLE (16729-081-10) | Jan 18, 2012 |
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