Orange Book product · Generic (ANDA)
RITODRINE HYDROCHLORIDE
RITODRINE HYDROCHLORIDE
At a glance
Feb 28, 1991
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Feb 28, 1991
35 yr 10 mo ago
Today
Pharmaceutical detail
Active ingredient
RITODRINE HYDROCHLORIDE
Strength
15MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 071619
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of RITODRINE HYDROCHLORIDE
- —YUTOPARBrand (NDA)
NDA 018580 · ASTRAZENECA
- —YUTOPARBrand (NDA)
NDA 018555 · ASTRAZENECA
- 1991RITODRINE HYDROCHLORIDEGeneric (ANDA)
ANDA 071618 · 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.
