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NDC 51862-0890-03 Azurette Details
Azurette
Azurette is a KIT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Mayne Pharma Inc.. The primary component is .
Product Information
NDC | 51862-0890 |
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Product ID | 51862-890_555bb0ac-47f9-4c8e-99e0-1c0e4b283b9a |
Associated GPIs | 25991002050320 |
GCN Sequence Number | 040125 |
GCN Sequence Number Description | desog-e.estradiol/e.estradiol TABLET 21-5 (28) ORAL |
HIC3 | G8A |
HIC3 Description | CONTRACEPTIVES,ORAL |
GCN | 94868 |
HICL Sequence Number | 018520 |
HICL Sequence Number Description | DESOGESTREL-ETHINYL ESTRADIOL/ETHINYL ESTRADIOL |
Brand/Generic | Generic |
Proprietary Name | Azurette |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | desogestrel/ethinyl estradiol and ethinyl estradiol |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | KIT |
Route | n/a |
Active Ingredient Strength | n/a |
Active Ingredient Units | n/a |
Substance Name | n/a |
Labeler Name | Mayne Pharma Inc. |
Pharmaceutical Class | n/a |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA091247 |
Listing Certified Through | 2024-12-31 |
Package
NDC 51862-0890-03 (51862089003)
NDC Package Code | 51862-890-03 |
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Billing NDC | 51862089003 |
Package | 3 BLISTER PACK in 1 CARTON (51862-890-03) / 1 KIT in 1 BLISTER PACK |
Marketing Start Date | 2020-10-03 |
NDC Exclude Flag | N |
Pricing Information | N/A |