Orange Book product · Brand (NDA)
MD-76R
DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM
At a glance
Sep 29, 1989
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 29, 1989
37 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM
Strength
66%;10%
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
NDA 019292
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
- —HYPAQUE-M,75%Brand (NDA)
NDA 010220 · GE HEALTHCARE
- —RENOGRAFIN-60Brand (NDA)
NDA 010040 · BRACCO
- —GASTROGRAFINBrand (NDA)
NDA 011245 · BRACCO
- 2023DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUMGeneric (ANDA)
ANDA 215049 · ANNORA PHARMA
- 2022DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUMGeneric (ANDA)
ANDA 214201 · ANDA REPOSITORY
- 1988RENOCAL-76Generic (ANDA)
ANDA 089347 · BRACCO
- 1983DIATRIZOATE-60Generic (ANDA)
ANDA 088166 · INTL MEDICATION
- 1982ANGIOVIST 292Generic (ANDA)
ANDA 087724 · BAYER HLTHCARE
- 1982ANGIOVIST 370Generic (ANDA)
ANDA 087723 · BAYER HLTHCARE
- 1982GASTROVISTGeneric (ANDA)
ANDA 087728 · BAYER HLTHCARE
- —HYPAQUE-76Generic (ANDA)
ANDA 086505 · GE HEALTHCARE
- —MD-60Generic (ANDA)
ANDA 087074 · MALLINCKRODT
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.
