NDC 70436-059 – Bupropion Hydrochloride SR
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC70436-059
Product details
- Brand name
- Bupropion Hydrochloride SR
- Generic name
- Bupropion hydrochloride
- Labeler
- Slate Run Pharmaceuticals, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211347
- Marketed since
- November 2, 2020
- Listing expires
- December 31, 2026
- 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 |
|---|---|---|
| 70436-059-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-01) | Nov 2, 2020 |
| 70436-059-02 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-02) | Nov 2, 2020 |
| 70436-059-05 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-05) | Nov 2, 2020 |
| 70436-059-22 | 250 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-22) | Nov 2, 2020 |
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