Orange Book product · Generic (ANDA)
AMMONIUM LACTATE
AMMONIUM LACTATE
At a glance
Jun 23, 2004
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 23, 2004
22 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
AMMONIUM LACTATE
Strength
EQ 12% BASE
Dosage form
LOTION
Route
TOPICAL
TE code
AB
Application
ANDA 075570
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of AMMONIUM LACTATE
- 1996LAC-HYDRINBrand (NDA)
NDA 020508 · SUN PHARM INDS INC
- 1985LAC-HYDRINBrand (NDA)
NDA 019155 · SUN PHARM INDS INC
- 2026AMMONIUM LACTATEGeneric (ANDA)
ANDA 217758 · ZYDUS LIFESCIENCES
- 2026AMMONIUM LACTATEGeneric (ANDA)
ANDA 217815 · ZYDUS LIFESCIENCES
- 2006AMMONIUM LACTATEGeneric (ANDA)
ANDA 076829 · WATSON LABS INC
- 2004AMMONIUM LACTATEGeneric (ANDA)
ANDA 076216 · SUN PHARMA CANADA
- 2003AMMONIUM LACTATEGeneric (ANDA)
ANDA 075883 · SUN PHARMA CANADA
- 2002AMMONIUM LACTATEGeneric (ANDA)
ANDA 075575 · WATSON LABS INC
- 2002AMMONIUM LACTATEGeneric (ANDA)
ANDA 075774 · PADAGIS ISRAEL
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.
