FDA Orange Book · active-ingredient family
Bendroflumethiazide; nadolol
Bendroflumethiazide; nadolol is approved as 1 brand and 2 generic applications in the FDA Orange Book, with their therapeutic-equivalence codes, listed patents, and marketing exclusivity.
Reference-listed drug:CORZIDE · NDA 018647
1
Brand (NDA)
2
Generics (ANDA)
0
Listed patents
0
Exclusivity periods
Brand (NDA) products · tablet
| Product | Applicant | Application | TE | Approved | |
|---|---|---|---|---|---|
| CORZIDERLD×2 | KING PHARMS LLC | NDA 018647 | — | May 25, 1983 |
Generic (ANDA) products (2)
| Product | Applicant | Application | TE | Approved | |
|---|---|---|---|---|---|
| NADOLOL AND BENDROFLUMETHIAZIDE×2 | NATCO PHARMA | ANDA 078688 | — | Feb 15, 2008 | |
| NADOLOL AND BENDROFLUMETHIAZIDE×2 | IMPAX LABS | ANDA 077833 | — | Mar 30, 2007 |
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.
Bendroflumethiazide; nadolol — frequently asked questions
Generics, reference-listed drug, patents, and exclusivity for this active ingredient, from the FDA Orange Book.

