NDC 0615-8504 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC0615-8504
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211020
- Marketed since
- August 1, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0615-8504-05 | 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8504-05) | Jul 16, 2024 |
| 0615-8504-39 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8504-39) | Mar 15, 2024 |
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