NDC 33342-527 – Bupropion Hydrochloride (SR)
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC33342-527
Product details
- Brand name
- Bupropion Hydrochloride (SR)
- Generic name
- Bupropion Hydrochloride
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA218567
- Marketed since
- June 23, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 33342-527-10 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-527-10) | Jun 23, 2026 |
| 33342-527-11 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-527-11) | Jun 23, 2026 |
| 33342-527-15 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-527-15) | Jun 23, 2026 |
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