NDC 70954-909 – Lofexidine
Lofexidine Hydrochloride .18 mg/1 · Tablet · Oral
Product NDC70954-909
Product details
- Brand name
- Lofexidine
- Generic name
- Lofexidine
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA219917
- Marketed since
- October 22, 2025
- Listing expires
- December 31, 2026
Active ingredients
- Lofexidine Hydrochloride .18 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 70954-909-10 | 36 TABLET in 1 BOTTLE (70954-909-10) | Oct 22, 2025 |
| 70954-909-20 | 96 TABLET in 1 BOTTLE (70954-909-20) | Oct 22, 2025 |