NDC 70518-2449

Ammonium Lactate

Ammonium Lactate

Ammonium Lactate is a Topical Cream in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Ammonium Lactate.

Product ID70518-2449_98371e57-e739-4132-e053-2995a90a79f3
NDC70518-2449
Product TypeHuman Prescription Drug
Proprietary NameAmmonium Lactate
Generic NameAmmonium Lactate
Dosage FormCream
Route of AdministrationTOPICAL
Marketing Start Date2019-11-25
Marketing CategoryANDA / ANDA
Application NumberANDA075774
Labeler NameREMEDYREPACK INC.
Substance NameAMMONIUM LACTATE
Active Ingredient Strength12 g/100g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 70518-2449-0

2 TUBE in 1 CARTON (70518-2449-0) > 140 g in 1 TUBE
Marketing Start Date2019-11-25
NDC Exclude FlagN
Sample Package?N

Drug Details

Active Ingredients

IngredientStrength
AMMONIUM LACTATE12 g/100g

NDC Crossover Matching brand name "Ammonium Lactate" or generic name "Ammonium Lactate"

NDCBrand NameGeneric Name
45802-419Ammonium LactateAmmonium Lactate
45802-493Ammonium LactateAmmonium Lactate
51672-1300Ammonium LactateAmmonium Lactate
51672-1301Ammonium LactateAmmonium Lactate
63044-404Ammonium LactateAmmonium Lactate
63044-484Ammonium LactateAmmonium Lactate
70518-2449Ammonium LactateAmmonium Lactate
10631-099Lac Hydrinammonium lactate

© 2019 FDA.report
This site is not affiliated with or endorsed by the FDA.