NDC 71335-0801 – Bupropion
Bupropion Hydrochloride 200 mg/1 · Tablet, Extended Release · Oral
Product NDC71335-0801
Product details
- Brand name
- Bupropion
- Generic name
- Bupropion hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202304
- Marketed since
- November 1, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 200 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0801-1 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-1) | May 1, 2018 |
| 71335-0801-2 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-2) | Aug 9, 2024 |
| 71335-0801-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-3) | Aug 9, 2024 |
| 71335-0801-4 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-4) | Aug 9, 2024 |
| 71335-0801-5 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-5) | Aug 9, 2024 |
| 71335-0801-6 | 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0801-6) | Aug 9, 2024 |
Other Bupropion products
- 63187-521 Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Proficient Rx LP
- 71205-565 Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Proficient Rx LP
- 65841-780 Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Zydus Lifesciences Limited
- 65841-836 Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Zydus Lifesciences Limited
- 68382-353 Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Zydus Pharmaceuticals USA Inc.
- 68382-354 Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Zydus Pharmaceuticals USA Inc.
- 51655-357 Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Northwind Health Company, LLC