NDC 71335-1214 – Bupropion Hydrochloride
Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral
Product NDC71335-1214
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210497
- Marketed since
- March 25, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 300 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1214-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-1) | May 3, 2019 |
| 71335-1214-2 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-2) | Apr 22, 2021 |
| 71335-1214-3 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-3) | Jun 10, 2019 |
| 71335-1214-4 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-4) | May 29, 2019 |
| 71335-1214-5 | 8 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-5) | Aug 9, 2024 |
| 71335-1214-6 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-6) | Aug 9, 2024 |
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