Orange Book product · Brand (NDA)
YUTOPAR
RITODRINE HYDROCHLORIDE
At a glance
Approved Prior to Jan 1, 1982
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
RITODRINE HYDROCHLORIDE
Strength
10MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
NDA 018555
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- —YUTOPARBrand (NDA)
NDA 018580 · ASTRAZENECA
- 1991RITODRINE HYDROCHLORIDEGeneric (ANDA)
ANDA 071618 · HOSPIRA
- 1991RITODRINE HYDROCHLORIDEGeneric (ANDA)
ANDA 071619 · HOSPIRA
- 1991RITODRINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINERGeneric (ANDA)
ANDA 071438 · HOSPIRA
- 1987RITODRINE HYDROCHLORIDEGeneric (ANDA)
ANDA 071188 · ABRAXIS PHARM
- 1987RITODRINE HYDROCHLORIDEGeneric (ANDA)
ANDA 071189 · ABRAXIS PHARM
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.
