Orange Book product · Generic (ANDA)
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
At a glance
Dec 18, 1986
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 18, 1986
40 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE
Strength
650MG;100MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 070399
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 077677 · WOCKHARDT LTD
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ANDA 077196 · WATSON LABS FLORIDA
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ANDA 076609 · WATSON LABS FLORIDA
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ANDA 076750 · CORNERSTONE
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ANDA 076743 · CORNERSTONE
- 2003DARVOCET A500Generic (ANDA)
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
- 1994PROPOXYPHENE NAPSYLATE AND ACETAMINOPHENGeneric (ANDA)
ANDA 074119 · TEVA
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.
