Orange Book product · Generic (ANDA)
CHLOROQUINE PHOSPHATE
CHLOROQUINE PHOSPHATE
At a glance
Jan 21, 2011
Approved
Generic (ANDA)
Application
AA
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 21, 2011
15 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
CHLOROQUINE PHOSPHATE
Strength
500MG
Dosage form
TABLET
Route
ORAL
TE code
AA
Application
ANDA 090612
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of CHLOROQUINE PHOSPHATE
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NDA 006002 · SANOFI AVENTIS US
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ANDA 214756 · SUVEN PHARMS
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ANDA 091621 · NATCO PHARMA LTD
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ANDA 090610 · IPCA LABS LTD
- 2009CHLOROQUINE PHOSPHATEGeneric (ANDA)
ANDA 090249 · IPCA LABS LTD
- 2003CHLOROQUINE PHOSPHATEGeneric (ANDA)
ANDA 040516 · IMPAX LABS
- 1982CHLOROQUINE PHOSPHATEGeneric (ANDA)
ANDA 087979 · WATSON LABS
- 1982CHLOROQUINE PHOSPHATEGeneric (ANDA)
ANDA 088030 · WATSON LABS
- 1982CHLOROQUINE PHOSPHATEGeneric (ANDA)
ANDA 087504 · TEVA
- —CHLOROQUINE PHOSPHATEGeneric (ANDA)
ANDA 083082 · HIKMA PHARMS
- —CHLOROQUINE PHOSPHATEGeneric (ANDA)
ANDA 080880 · IMPAX LABS
- —CHLOROQUINE PHOSPHATEGeneric (ANDA)
ANDA 087228 · MD 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.
