NDC 71205-968 – Bupropion Hydrochloride (XL)
Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral
Product NDC71205-968
Product details
- Brand name
- Bupropion Hydrochloride (XL)
- Generic name
- Bupropion hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210081
- Marketed since
- August 30, 2018
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 71205-968-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-968-30) | Jun 9, 2020 |
| 71205-968-55 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-968-55) | Jun 9, 2020 |
| 71205-968-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-968-90) | Jun 9, 2020 |
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