NDC 46708-317 – Desipramine Hydrochloride
Desipramine Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral
Product NDC46708-317
Product details
- Brand name
- Desipramine Hydrochloride
- Generic name
- Desipramine Hydrochloride
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209785
- Marketed since
- July 8, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Tricyclic Antidepressant
Active ingredients
- Desipramine Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Desipramine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 46708-317-30 | 30 TABLET, FILM COATED in 1 BOTTLE (46708-317-30) | Jul 8, 2021 |
| 46708-317-31 | 100 TABLET, FILM COATED in 1 BOTTLE (46708-317-31) | Jul 8, 2021 |
| 46708-317-91 | 1000 TABLET, FILM COATED in 1 BOTTLE (46708-317-91) | Jul 8, 2021 |
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- 62332-317 Desipramine Hydrochloride 50 mg/1 · Tablet, Film Coated · Alembic Pharmaceuticals Inc.
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- 62332-320 Desipramine Hydrochloride 150 mg/1 · Tablet, Film Coated · Alembic Pharmaceuticals Inc.