Orange Book product · Generic (ANDA)
PENTOBARBITAL SODIUM
PENTOBARBITAL SODIUM
At a glance
May 23, 2016
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 23, 2016
10 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
PENTOBARBITAL SODIUM
Strength
50MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 206404
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of PENTOBARBITAL SODIUM
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ANDA 206677 · BPI LABS
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ANDA 203619 · HIKMA
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ANDA 083247 · SCIEGEN PHARMS
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ANDA 084095 · EPIC PHARMA LLC
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ANDA 084093 · EPIC PHARMA LLC
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ANDA 083245 · EPIC PHARMA LLC
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ANDA 085937 · LANNETT
- —PENTOBARBITAL SODIUMGeneric (ANDA)
ANDA 085915 · LANNETT
- —PENTOBARBITAL SODIUMGeneric (ANDA)
ANDA 083284 · VITARINE
- —PENTOBARBITAL SODIUMGeneric (ANDA)
ANDA 083338 · WHITEWORTH TOWN PLSN
- —SODIUM PENTOBARBITALGeneric (ANDA)
ANDA 084590 · ANABOLIC
- —SODIUM PENTOBARBITALGeneric (ANDA)
ANDA 083368 · ELKINS SINN
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.
