NDC 47335-954 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC47335-954
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA200695
- Marketed since
- December 25, 2014
- 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 |
|---|---|---|
| 47335-954-13 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-13) | Dec 25, 2014 |
| 47335-954-81 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-81) | Dec 25, 2014 |
| 47335-954-83 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-83) | Dec 25, 2014 |
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