NDC 70771-1528 – Doxepin
Doxepin Hydrochloride 3 mg/1 · Tablet · Oral
Product NDC70771-1528
Product details
- Brand name
- Doxepin
- Generic name
- Doxepin
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202761
- Marketed since
- June 30, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Tricyclic Antidepressant
Active ingredients
- Doxepin Hydrochloride 3 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1528-0 | 1000 TABLET in 1 BOTTLE (70771-1528-0) | Jun 30, 2024 |
| 70771-1528-1 | 100 TABLET in 1 BOTTLE (70771-1528-1) | Jun 30, 2024 |
| 70771-1528-3 | 30 TABLET in 1 BOTTLE (70771-1528-3) | Jun 30, 2024 |
| 70771-1528-4 | 10 BLISTER PACK in 1 CARTON (70771-1528-4) / 10 TABLET in 1 BLISTER PACK | Jun 30, 2024 |
| 70771-1528-5 | 500 TABLET in 1 BOTTLE (70771-1528-5) | Jun 30, 2024 |
| 70771-1528-9 | 90 TABLET in 1 BOTTLE (70771-1528-9) | Jun 30, 2024 |
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