NDC 85534-0006 – Bupropion Hydrochloride
Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral
Product NDC85534-0006
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- HAWAII REPACK, INC.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077285
- Marketed since
- February 17, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 300 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 85534-0006-1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-1) | Jun 11, 2025 |
| 85534-0006-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-3) | Jun 11, 2025 |
| 85534-0006-5 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-5) | Jun 11, 2025 |
| 85534-0006-6 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-6) | Jun 11, 2025 |
| 85534-0006-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-9) | Jun 11, 2025 |
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