NDC 69315-134 – Imipramine Hydrochloride
Imipramine Hydrochloride 25 mg/1 · Tablet, Film Coated · Oral
Product NDC69315-134
Product details
- Brand name
- Imipramine Hydrochloride
- Generic name
- Imipramine Hydrochloride
- Labeler
- Leading Pharma, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA040903
- Marketed since
- April 7, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Tricyclic Antidepressant
Active ingredients
- Imipramine Hydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Imipramine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 69315-134-01 | 100 TABLET, FILM COATED in 1 BOTTLE (69315-134-01) | Apr 12, 2016 |
| 69315-134-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (69315-134-10) | May 1, 2016 |
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