Orange Book product · Generic (ANDA)
NALOXONE HYDROCHLORIDE
NALOXONE HYDROCHLORIDE
At a glance
Apr 11, 1989
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 11, 1989
37 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
NALOXONE HYDROCHLORIDE
Strength
0.02MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 072081
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of NALOXONE HYDROCHLORIDE
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ANDA 213279 · EUGIA PHARMA
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- 2018NALOXONE HYDROCHLORIDEGeneric (ANDA)
ANDA 207846 · CHARTWELL RX
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ANDA 072082 · IGI LABS INC
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.
