NDC 21695-892

Econazole Nitrate

Econazole Nitrate

Econazole Nitrate is a Topical Cream in the Human Prescription Drug category. It is labeled and distributed by Rebel Distributors Corp. The primary component is Econazole Nitrate.

Product ID21695-892_28e567ca-dd90-45cc-894c-330437497531
NDC21695-892
Product TypeHuman Prescription Drug
Proprietary NameEconazole Nitrate
Generic NameEconazole Nitrate
Dosage FormCream
Route of AdministrationTOPICAL
Marketing Start Date2004-06-23
Marketing CategoryANDA / ANDA
Application NumberANDA076479
Labeler NameRebel Distributors Corp
Substance NameECONAZOLE NITRATE
Active Ingredient Strength10 mg/g
Pharm ClassesAzole Antifungal [EPC],Azoles [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 21695-892-85

85 g in 1 TUBE (21695-892-85)
Marketing Start Date2004-06-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 21695-892-85 [21695089285]

Econazole Nitrate CREAM
Marketing CategoryANDA
Application NumberANDA076479
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date2004-06-23
Inactivation Date2019-09-24

NDC 21695-892-15 [21695089215]

Econazole Nitrate CREAM
Marketing CategoryANDA
Application NumberANDA076479
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date2004-06-23
Inactivation Date2019-09-24

NDC 21695-892-30 [21695089230]

Econazole Nitrate CREAM
Marketing CategoryANDA
Application NumberANDA076479
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitGM
Marketing Start Date2004-06-23
Inactivation Date2019-09-24

Drug Details

Active Ingredients

IngredientStrength
ECONAZOLE NITRATE10 mg/g

OpenFDA Data

SPL SET ID:28e567ca-dd90-45cc-894c-330437497531
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 857366

    • Pharmacological Class

    • Azole Antifungal [EPC]
    • Azoles [CS]