NDC 0591-5714 – Amoxapine
Amoxapine 50 mg/1 · Tablet · Oral
Product NDC0591-5714
Product details
- Brand name
- Amoxapine
- Generic name
- Amoxapine
- Labeler
- Actavis Pharma, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA072691
- Marketed since
- August 28, 1992
- Listing expires
- December 31, 2027
- Pharmacologic class
- Tricyclic Antidepressant
Active ingredients
- Amoxapine 50 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0591-5714-01 | 100 TABLET in 1 BOTTLE, PLASTIC (0591-5714-01) | Aug 28, 1992 |
Other Amoxapine products
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- 0591-5715 Amoxapine 100 mg/1 · Tablet · Actavis Pharma, Inc.
- 0591-5716 Amoxapine 150 mg/1 · Tablet · Actavis Pharma, Inc.
- 62135-700 Amoxapine 25 mg/1 · Tablet · Chartwell RX, LLC
- 62135-701 Amoxapine 50 mg/1 · Tablet · Chartwell RX, LLC
- 62135-702 Amoxapine 100 mg/1 · Tablet · Chartwell RX, LLC
- 62135-703 Amoxapine 150 mg/1 · Tablet · Chartwell RX, LLC