NDC 42806-096 – Protriptyline Hydrochloride
Protriptyline Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC42806-096
Product details
- Brand name
- Protriptyline Hydrochloride
- Generic name
- Protriptyline Hydrochloride
- Labeler
- Epic Pharma, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202220
- Marketed since
- January 9, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Tricyclic Antidepressant
Active ingredients
- Protriptyline Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Protriptyline Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 42806-096-01 | 100 TABLET, FILM COATED in 1 BOTTLE (42806-096-01) | Jan 9, 2013 |
| 42806-096-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (42806-096-10) | Jan 9, 2013 |
| 42806-096-30 | 30 TABLET, FILM COATED in 1 BOTTLE (42806-096-30) | Jul 10, 2020 |