NDC 70436-010 – Bupropion Hydrochloride XL
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC70436-010
Product details
- Brand name
- Bupropion Hydrochloride XL
- Generic name
- Bupropion hydrochloride
- Labeler
- Slate Run Pharmaceuticals, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210015
- Marketed since
- December 1, 2018
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 70436-010-02 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70436-010-02) | Dec 1, 2018 |
| 70436-010-04 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70436-010-04) | Dec 1, 2018 |
| 70436-010-06 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70436-010-06) | Dec 1, 2018 |
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