NDC 76420-923 – Bupropion Hydrochloride XL
Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC76420-923
Product details
- Brand name
- Bupropion Hydrochloride XL
- Generic name
- Bupropion Hydrochloride
- Labeler
- Asclemed USA, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077715
- Marketed since
- November 26, 2008
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 76420-923-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (76420-923-01) | Feb 25, 2025 |
| 76420-923-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (76420-923-05) | Feb 25, 2025 |
| 76420-923-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (76420-923-30) | Feb 25, 2025 |
| 76420-923-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (76420-923-60) | Feb 25, 2025 |
| 76420-923-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (76420-923-90) | Feb 25, 2025 |
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