Orange Book product · Generic (ANDA)
SUCRALFATE
SUCRALFATE
At a glance
Apr 15, 2022
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 15, 2022
4 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
SUCRALFATE
Strength
1GM
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 215576
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
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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.
