NDC 66993-345 – Lofexidine hydrochloride
Lofexidine Hydrochloride .2 mg/1 · Tablet, Film Coated · Oral
Product NDC66993-345
Product details
- Brand name
- Lofexidine hydrochloride
- Generic name
- Lofexidine hydrochloride
- Labeler
- Prasco Laboratories
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA209229
- Marketed since
- August 29, 2024
- Marketing end
- June 30, 2027
Active ingredients
- Lofexidine Hydrochloride .2 mg/1
Uses, dosage, side effects and warnings for Lofexidine hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 66993-345-37 | 1 BOTTLE in 1 CARTON (66993-345-37) / 36 TABLET, FILM COATED in 1 BOTTLE | Aug 29, 2024 |
| 66993-345-76 | 1 BOTTLE in 1 CARTON (66993-345-76) / 96 TABLET, FILM COATED in 1 BOTTLE | Aug 29, 2024 |
Other Lofexidine hydrochloride products
- 72205-246 Lofexidine Hydrochloride .2 mg/1 · Tablet, Film Coated · Novadoz Pharmaceuticals LLC