NDC 70518-2718 – Naltrexone Hydrochloride
Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC70518-2718
Product details
- Brand name
- Naltrexone Hydrochloride
- Generic name
- Naltrexone Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090356
- Marketed since
- May 1, 2020
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 70518-2718-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2718-0) | May 1, 2020 |
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