NDC 70710-1235

Desonide

Desonide

Desonide is a Topical Cream in the Human Prescription Drug category. It is labeled and distributed by Zydus Pharmaceuticals (usa) Inc.. The primary component is Desonide.

Product ID70710-1235_54d6a235-719a-488a-bdbf-234d7e890f81
NDC70710-1235
Product TypeHuman Prescription Drug
Proprietary NameDesonide
Generic NameDesonide
Dosage FormCream
Route of AdministrationTOPICAL
Marketing Start Date2019-11-25
Marketing CategoryANDA / ANDA
Application NumberANDA210198
Labeler NameZydus Pharmaceuticals (USA) Inc.
Substance NameDESONIDE
Active Ingredient Strength1 mg/g
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 70710-1235-3

1 TUBE in 1 CARTON (70710-1235-3) > 60 g in 1 TUBE
Marketing Start Date2019-11-25
NDC Exclude FlagN
Sample Package?N

Drug Details

Active Ingredients

IngredientStrength
DESONIDE.5 mg/g

Pharmacological Class

  • Corticosteroid [EPC]
  • Corticosteroid Hormone Receptor Agonists [MoA]

NDC Crossover Matching brand name "Desonide" or generic name "Desonide"

NDCBrand NameGeneric Name
10922-828DESONATEdesonide
50222-504DESONATEdesonide
50419-828DESONATEdesonide
0115-1517DesonideDesonide
0168-0309desonidedesonide
0168-0310desonidedesonide
0472-0803Desonidedesonide
0472-0804Desonidedesonide
0713-0661DesonideDesonide
16714-729DesonideDesonide
16714-828DesonideDesonide
21695-944DESONIDEDESONIDE
42254-142DesonideDesonide
45802-422DesonideDesonide
45802-423DesonideDesonide
51672-1280DesonideDesonide
51672-1281DesonideDesonide
51672-4079DesonideDesonide
52565-038DesonideDesonide
61748-470DesonideDesonide
63187-747DesonideDesonide
68462-252DesonideDesonide
68462-513desonidedesonide
68462-528DesonideDesonide
69007-765desonidedesonide
69007-770desonidedesonide
62332-485DesonideDesonide
71589-005DesonideDesonide
70710-1235DesonideDesonide
0299-5765DesOwendesonide
0299-5770DesOwendesonide
0462-0392LoKaradesonide
16110-111Verdesodesonide

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