NDC 62135-700 – Amoxapine
Amoxapine 25 mg/1 · Tablet · Oral
Product NDC62135-700
Product details
- Brand name
- Amoxapine
- Generic name
- Amoxapine
- Labeler
- Chartwell RX, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA072879
- Marketed since
- June 28, 1991
- Listing expires
- December 31, 2026
- Pharmacologic class
- Tricyclic Antidepressant
Active ingredients
- Amoxapine 25 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 62135-700-90 | 90 TABLET in 1 BOTTLE (62135-700-90) | Sep 6, 2023 |
Other Amoxapine products
- 0591-5713 Amoxapine 25 mg/1 · Tablet · Actavis Pharma, Inc.
- 0591-5714 Amoxapine 50 mg/1 · Tablet · Actavis Pharma, Inc.
- 0591-5715 Amoxapine 100 mg/1 · Tablet · Actavis Pharma, Inc.
- 0591-5716 Amoxapine 150 mg/1 · Tablet · Actavis Pharma, Inc.
- 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