Orange Book product · Generic (ANDA)
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
At a glance
Dec 19, 1994
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 19, 1994
32 yr ago
Today
Pharmaceutical detail
Active ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Strength
650MG;100MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 074119
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
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ANDA 076609 · WATSON LABS FLORIDA
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ANDA 076750 · CORNERSTONE
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ANDA 076743 · CORNERSTONE
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ANDA 076429 · XANODYNE PHARM
- 2001PROPOXYPHENE NAPSYLATE AND ACETAMINOPHENGeneric (ANDA)
ANDA 075838 · ABLE
- 2001PROPOXYPHENE NAPSYLATE AND ACETAMINOPHENGeneric (ANDA)
ANDA 074843 · VINTAGE PHARMS
- 2001PROPOXYPHENE NAPSYLATE AND ACETAMINOPHENGeneric (ANDA)
ANDA 075738 · MALLINCKRODT
- 1988PROPOXYPHENE NAPSYLATE AND ACETAMINOPHENGeneric (ANDA)
ANDA 072105 · HALSEY
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.
