NDC 72205-246 – Lofexidine hydrochloride
Lofexidine Hydrochloride .2 mg/1 · Tablet, Film Coated · Oral
Product NDC72205-246
Product details
- Brand name
- Lofexidine hydrochloride
- Generic name
- Lofexidine hydrochloride
- Labeler
- Novadoz Pharmaceuticals LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA218699
- Marketed since
- February 24, 2025
- Listing expires
- December 31, 2026
Active ingredients
- Lofexidine Hydrochloride .2 mg/1
Uses, dosage, side effects and warnings for Lofexidine hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72205-246-42 | 1 BOTTLE in 1 CARTON (72205-246-42) / 36 TABLET, FILM COATED in 1 BOTTLE | Mar 1, 2025 |
| 72205-246-43 | 1 BOTTLE in 1 CARTON (72205-246-43) / 96 TABLET, FILM COATED in 1 BOTTLE | Mar 1, 2025 |
Other Lofexidine hydrochloride products
- 66993-345 Lofexidine Hydrochloride .2 mg/1 · Tablet, Film Coated · Prasco Laboratories