NDC 72516-035 – buPropion Hydrochloride XL
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC72516-035
Product details
- Brand name
- buPropion Hydrochloride XL
- Generic name
- Bupropion hydrochloride
- Labeler
- Oryza pharmaceuticals Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211200
- Marketed since
- October 1, 2020
- 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 |
|---|---|---|
| 72516-035-03 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-035-03) | Oct 1, 2020 |
| 72516-035-09 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-035-09) | Oct 1, 2020 |
| 72516-035-50 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72516-035-50) | Oct 1, 2020 |
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