NDC 68084-291 – Naltrexone Hydrochloride
Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC68084-291
Product details
- Brand name
- Naltrexone Hydrochloride
- Generic name
- Naltrexone hydrochloride
- Labeler
- American Health Packaging
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076264
- Marketed since
- June 3, 2013
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 68084-291-21 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-291-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-291-11) | Jun 3, 2013 |
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