Orange Book product · Generic (ANDA)
SUCRALFATE
SUCRALFATE
At a glance
Dec 02, 2019
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 02, 2019
6 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
SUCRALFATE
Strength
1GM/10ML
Dosage form
SUSPENSION
Route
ORAL
TE code
AB
Application
ANDA 209356
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.
