NDC 67046-0699 – Bupropion Hydrochloride XL
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC67046-0699
Product details
- Brand name
- Bupropion Hydrochloride XL
- Generic name
- Bupropion Hydrochloride
- Labeler
- Coupler LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090693
- Marketed since
- May 6, 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 67046-0699-3 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-0699-3) | May 6, 2026 |
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