NDC 68094-853 – Naltrexone Hydrochloride
Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC68094-853
Product details
- Brand name
- Naltrexone Hydrochloride
- Generic name
- naltrexone Hydrochloride
- Labeler
- Precision Dose Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075274
- Marketed since
- October 29, 2014
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 68094-853-61 | 10 BLISTER PACK in 1 CARTON (68094-853-61) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59) | Aug 15, 2024 |
| 68094-853-62 | 3 BLISTER PACK in 1 CARTON (68094-853-62) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59) | Oct 29, 2014 |
| 68094-853-66 | 2 BLISTER PACK in 1 CARTON (68094-853-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59) | Aug 15, 2024 |
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