NDC 51655-098 – Bupropion Hydrochloride XL
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC51655-098
Product details
- Brand name
- Bupropion Hydrochloride XL
- Generic name
- Bupropion Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090693
- Marketed since
- September 6, 2022
- 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 |
|---|---|---|
| 51655-098-26 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-098-26) | Sep 6, 2022 |
| 51655-098-52 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-098-52) | Apr 7, 2023 |
| 51655-098-83 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-098-83) | Jan 3, 2023 |
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