NDC 70518-2458 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC70518-2458
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210497
- Marketed since
- November 29, 2019
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 70518-2458-0 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2458-0) | Nov 29, 2019 |
| 70518-2458-2 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2458-2) | Jul 6, 2020 |
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