NDC 50090-5101 – Bupropion Hydrochloride (sr)
Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC50090-5101
Product details
- Brand name
- Bupropion Hydrochloride (sr)
- Generic name
- Bupropion Hydrochloride
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA206122
- Marketed since
- August 17, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Bupropion Hydrochloride (sr) →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 50090-5101-0 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5101-0) | Jul 13, 2020 |
| 50090-5101-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5101-1) | Jul 13, 2020 |
Other Bupropion Hydrochloride (sr) products
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- 69097-878 Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Cipla USA Inc.,
- 69097-879 Bupropion Hydrochloride 200 mg/1 · Tablet, Extended Release · Cipla USA Inc.,
- 43598-863 Bupropion Hydrochloride 150 mg/1 · Tablet, Extended Release · Dr. Reddy's Laboratories Inc
- 72189-349 Bupropion Hydrochloride 150 mg/1 · Tablet, Film Coated, Extended Release · DirectRx