NDC 72789-158 – Bupropion Hydrochloride SR
Bupropion Hydrochloride 100 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC72789-158
Product details
- Brand name
- Bupropion Hydrochloride SR
- Generic name
- bupropion hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA205794
- Marketed since
- April 20, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 100 mg/1
Uses, dosage, side effects and warnings for bupropion hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72789-158-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-158-60) | Jan 18, 2021 |
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