NDC 42806-415 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC42806-415
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Epic Pharma LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA075932
- Marketed since
- December 15, 2021
- 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 |
|---|---|---|
| 42806-415-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-415-01) | Dec 15, 2021 |
| 42806-415-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-415-05) | Dec 15, 2021 |
| 42806-415-52 | 250 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-415-52) | Dec 15, 2021 |
| 42806-415-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-415-60) | Dec 15, 2021 |
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