NDC 47335-326 – Naltrexone Hydrochloride
Naltrexone Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC47335-326
Product details
- Brand name
- Naltrexone Hydrochloride
- Generic name
- Naltrexone Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090356
- Marketed since
- February 29, 2012
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 47335-326-08 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-326-08) | Feb 29, 2012 |
| 47335-326-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18) | Feb 29, 2012 |
| 47335-326-83 | 30 TABLET, FILM COATED in 1 BOTTLE (47335-326-83) | Feb 29, 2012 |
| 47335-326-88 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-326-88) | Feb 29, 2012 |
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