NDC 65841-836 – Bupropion
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC65841-836
Product details
- Brand name
- Bupropion
- Generic name
- Bupropion
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA201567
- Marketed since
- August 2, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 65841-836-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-05) | Aug 2, 2018 |
| 65841-836-06 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-06) | Aug 2, 2018 |
| 65841-836-10 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-10) | Aug 2, 2018 |
| 65841-836-16 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-16) | Aug 2, 2018 |
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