NDC 51655-115 – Bupropion Hydrochloride SR
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC51655-115
Product details
- Brand name
- Bupropion Hydrochloride SR
- Generic name
- Bupropion hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211347
- Marketed since
- October 5, 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 51655-115-25 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-25) | Oct 5, 2022 |
| 51655-115-26 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-26) | Nov 15, 2022 |
| 51655-115-52 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-52) | Nov 30, 2022 |
| 51655-115-83 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-115-83) | Jan 5, 2023 |
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