Orange Book product · Generic (ANDA)
AMINOPHYLLINE
AMINOPHYLLINE
At a glance
Jul 23, 1982
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jul 23, 1982
44 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
AMINOPHYLLINE
Strength
25MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 087601
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
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 087242 · HOSPIRA
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.
