NDC 70010-784 – Bupropion hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC70010-784
Product details
- Brand name
- Bupropion hydrochloride
- Generic name
- Bupropion hydrochloride
- Labeler
- Granules Pharmaceuticals Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA215568
- Marketed since
- December 15, 2022
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 70010-784-03 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-784-03) | Dec 15, 2022 |
| 70010-784-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-784-05) | Dec 15, 2022 |
| 70010-784-09 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-784-09) | Dec 15, 2022 |
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