Orange Book product · Generic (ANDA)
BUPROPION HYDROCHLORIDE
BUPROPION HYDROCHLORIDE
At a glance
May 04, 2026
Approved
Generic (ANDA)
Application
AB1
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 04, 2026
2 mo ago
Today
Pharmaceutical detail
Active ingredient
BUPROPION HYDROCHLORIDE
Strength
100MG
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
TE code
AB1
Application
ANDA 220529
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of BUPROPION HYDROCHLORIDE
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ANDA 203650 · SUN PHARM
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ANDA 200216 · SUN PHARM
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ANDA 211200 · ZHEJIANG JUTAI PHARM
- 2019BUPROPION HYDROCHLORIDEGeneric (ANDA)
ANDA 211020 · GRAVITI PHARMS
- 2018BUPROPION HYDROCHLORIDEGeneric (ANDA)
ANDA 210497 · ACCORD HLTHCARE
- 2018BUPROPION HYDROCHLORIDEGeneric (ANDA)
ANDA 211347 · YICHANG HUMANWELL
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.

