NDC 51672-4002 – Nortriptyline Hydrochloride
Nortriptyline Hydrochloride 25 mg/1 · Capsule · Oral
Product NDC51672-4002
Product details
- Brand name
- Nortriptyline Hydrochloride
- Generic name
- Nortriptyline Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA075520
- Marketed since
- May 8, 2000
- Listing expires
- December 31, 2027
- Pharmacologic class
- Tricyclic Antidepressant
Active ingredients
- Nortriptyline Hydrochloride 25 mg/1
Uses, dosage, side effects and warnings for Nortriptyline Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4002-1 | 100 CAPSULE in 1 BOTTLE (51672-4002-1) | May 8, 2000 |
| 51672-4002-2 | 500 CAPSULE in 1 BOTTLE (51672-4002-2) | May 8, 2000 |
| 51672-4002-4 | 60 CAPSULE in 1 BOTTLE (51672-4002-4) | May 8, 2000 |
| 51672-4002-5 | 90 CAPSULE in 1 BOTTLE (51672-4002-5) | May 8, 2000 |
| 51672-4002-6 | 30 CAPSULE in 1 BOTTLE (51672-4002-6) | May 8, 2000 |
Recalls mentioning this NDC
- D-0246-2021 Feb 10, 2021 · Class II
CGMP deviations.
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