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    NDC 10631-0007-31 Absorica LD 32 mg/1 Details

    Absorica LD 32 mg/1

    Absorica LD is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is ISOTRETINOIN.

    Product Information

    NDC 10631-0007
    Product ID 10631-007_fba81535-0761-42a7-b422-338f8bd2cfc6
    Associated GPIs 90050013100135
    GCN Sequence Number 080454
    GCN Sequence Number Description isotretinoin, micronized CAPSULE 32 MG ORAL
    HIC3 L1B
    HIC3 Description ACNE AGENTS,SYSTEMIC
    GCN 47302
    HICL Sequence Number 046198
    HICL Sequence Number Description ISOTRETINOIN, MICRONIZED
    Brand/Generic Brand
    Proprietary Name Absorica LD
    Proprietary Name Suffix n/a
    Non-Proprietary Name isotretinoin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 32
    Active Ingredient Units mg/1
    Substance Name ISOTRETINOIN
    Labeler Name Sun Pharmaceutical Industries, Inc.
    Pharmaceutical Class Retinoid [EPC], Retinoids [CS]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA211913
    Listing Certified Through 2024-12-31

    Package

    NDC 10631-0007-31 (10631000731)

    NDC Package Code 10631-007-31
    Billing NDC 10631000731
    Package 3 BLISTER PACK in 1 BOX (10631-007-31) / 10 CAPSULE in 1 BLISTER PACK
    Marketing Start Date 2019-11-20
    NDC Exclude Flag N
    Pricing Information N/A