NDC 69097-917 – bupropion Hydrochloride
Bupropion Hydrochloride 75 mg/1 · Tablet · Oral
Product NDC69097-917
Product details
- Brand name
- bupropion Hydrochloride
- Generic name
- bupropion Hydrochloride
- Labeler
- CIPLA USA INC.,
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA207389
- Marketed since
- May 26, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 75 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 69097-917-02 | 30 TABLET in 1 BOTTLE (69097-917-02) | May 26, 2018 |
| 69097-917-07 | 100 TABLET in 1 BOTTLE (69097-917-07) | May 26, 2018 |
| 69097-917-15 | 1000 TABLET in 1 BOTTLE (69097-917-15) | May 26, 2018 |
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