Orange Book product · Generic (ANDA)
AMINOPHYLLINE
AMINOPHYLLINE
At a glance
Oct 26, 1983
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 26, 1983
43 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
AMINOPHYLLINE
Strength
25MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 087242
Product number
001
Marketing status
RX
Reference listed drug (RLD)
Yes
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of AMINOPHYLLINE
- 1984AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINERBrand (NDA)
NDA 018924 · HOSPIRA
- 1982SOMOPHYLLINBrand (NDA)
NDA 018232 · FISONS
- —AMINOPHYLLINBrand (NDA)
NDA 002386 · GD SEARLE LLC
- 1991AMINOPHYLLINEGeneric (ANDA)
ANDA 081142 · TEVA PARENTERAL
- 1985AMINOPHYLLINEGeneric (ANDA)
ANDA 088429 · SMITH AND NEPHEW
- 1985AMINOPHYLLINEGeneric (ANDA)
ANDA 088749 · SMITH AND NEPHEW
- 1984AMINOPHYLLINEGeneric (ANDA)
ANDA 088407 · ABRAXIS PHARM
- 1983AMINOPHYLLINEGeneric (ANDA)
ANDA 087392 · PHARMA SERVE NY
- 1983AMINOPHYLLINEGeneric (ANDA)
ANDA 088156 · MORTON GROVE
- 1983AMINOPHYLLINEGeneric (ANDA)
ANDA 087867 · INTL MEDICATION
- 1983AMINOPHYLLINEGeneric (ANDA)
ANDA 087868 · INTL MEDICATION
- 1983AMINOPHYLLINEGeneric (ANDA)
ANDA 087886 · 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.
