NDC 71335-2312 – Bupropion Hydrochloride (XL)
Bupropion Hydrochloride 300 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC71335-2312
Product details
- Brand name
- Bupropion Hydrochloride (XL)
- Generic name
- Bupropion hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA207479
- Marketed since
- April 12, 2017
- 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 |
|---|---|---|
| 71335-2312-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-1) | Dec 21, 2023 |
| 71335-2312-2 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-2) | Dec 21, 2023 |
| 71335-2312-3 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-3) | Dec 21, 2023 |
| 71335-2312-4 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-4) | Dec 21, 2023 |
| 71335-2312-5 | 8 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-5) | Dec 21, 2023 |
| 71335-2312-6 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-6) | Dec 21, 2023 |
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