NDC 85789-901 – Lofexidine
Lofexidine Hydrochloride .2 mg/1 · Tablet, Film Coated · Oral
Product NDC85789-901
Product details
- Brand name
- Lofexidine
- Generic name
- Lofexidine hydrochloride
- Labeler
- BioCorRx Pharmaceuticals Inc
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA · NDA209229
- Marketed since
- August 15, 2026
- Listing expires
- December 31, 2027
Active ingredients
- Lofexidine Hydrochloride .2 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 85789-901-36 | 36 TABLET, FILM COATED in 1 BOTTLE (85789-901-36) | Aug 15, 2026 |
| 85789-901-96 | 96 TABLET, FILM COATED in 1 BOTTLE (85789-901-96) | Aug 15, 2026 |