NDC 51655-357 – bupropion
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC51655-357
Product details
- Brand name
- bupropion
- Generic name
- bupropion hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202304
- Marketed since
- May 28, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51655-357-26 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-357-26) | May 28, 2020 |
| 51655-357-52 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-357-52) | Sep 1, 2022 |
Other bupropion products
- 71335-0801 Bupropion Hydrochloride 200 mg/1 · Tablet, Extended Release · Bryant Ranch Prepack
- 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.