NDC 72789-301 – Bupropion Hydrochloride
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC72789-301
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA210497
- Marketed since
- November 8, 2018
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 72789-301-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-301-90) | Feb 22, 2022 |
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