NDC 62032-414

Tretinoin Cream

Tretinoin

Tretinoin Cream is a Topical Cream in the Human Prescription Drug category. It is labeled and distributed by Obagi Cosmeceuticals Llc. The primary component is Tretinoin.

Product ID62032-414_0af0de52-f69b-4ad2-a6a2-cf51720bc039
NDC62032-414
Product TypeHuman Prescription Drug
Proprietary NameTretinoin Cream
Generic NameTretinoin
Dosage FormCream
Route of AdministrationTOPICAL
Marketing Start Date1988-09-16
Marketing CategoryNDA / NDA
Application NumberNDA019049
Labeler NameObagi Cosmeceuticals LLC
Substance NameTRETINOIN
Active Ingredient Strength0 mg/g
Pharm ClassesRetinoid [EPC],Retinoids [CS]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 62032-414-20

1 TUBE in 1 CARTON (62032-414-20) > 20 g in 1 TUBE
Marketing Start Date1988-09-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62032-414-20 [62032041420]

Tretinoin Cream CREAM
Marketing CategoryNDA
Application NumberNDA019049
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1988-09-16

Drug Details

Active Ingredients

IngredientStrength
TRETINOIN.25 mg/g

OpenFDA Data

SPL SET ID:745cc3ce-60b4-4479-a055-316817567949
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 106302
  • 106303
  • 198300
  • Pharmacological Class

    • Retinoid [EPC]
    • Retinoids [CS]
    • Retinoid [EPC]
    • Retinoids [CS]

    NDC Crossover Matching brand name "Tretinoin Cream" or generic name "Tretinoin"

    NDCBrand NameGeneric Name
    62032-412Tretinoin CreamTretinoin Cream
    62032-414Tretinoin CreamTretinoin Cream
    62032-417Tretinoin CreamTretinoin Cream
    0187-0005Altrenotretinoin
    0187-5150RenovaTretinoin
    0187-5160Retin-ATretinoin
    0187-5162Retin-ATretinoin
    0187-5164Retin-ATretinoin
    0187-5140Retin-A MICROTretinoin
    0187-5144Retin-A MICROTretinoin
    0187-5146Retin-A MICROTretinoin
    0187-5148Retin-A MICROTretinoin

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