aubra eq

Generic: levonorgestrel and ethinyl estradiol

Labeler: afaxys pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aubra eq
Generic Name levonorgestrel and ethinyl estradiol
Labeler afaxys pharma, llc
Dosage Form KIT
Manufacturer
Afaxys Pharma, LLC

Identifiers & Regulatory

Product NDC 50102-220
Product ID 50102-220_168ba8ff-87c7-4c10-a48d-6fe29555a997
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206886
Listing Expiration 2026-12-31
Marketing Start 2016-11-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50102220
Hyphenated Format 50102-220

Supplemental Identifiers

RxCUI
242297 748797 748868 1440185

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name aubra eq (source: ndc)
Generic Name levonorgestrel and ethinyl estradiol (source: ndc)
Application Number ANDA206886 (source: ndc)

Resolved Composition

Strengths
  • 0.1 mg/0.02 mg
source: label
Packaging
  • 3 POUCH in 1 CARTON (50102-220-23) / 1 BLISTER PACK in 1 POUCH (50102-220-21) / 1 KIT in 1 BLISTER PACK
source: ndc

Packages (1)

50102-220-23 3 POUCH in 1 CARTON (50102-220-23) / 1 BLISTER PACK in 1 POUCH (50102-220-21) / 1 KIT in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Aubra EQ ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "168ba8ff-87c7-4c10-a48d-6fe29555a997", "openfda": {"rxcui": ["242297", "748797", "748868", "1440185"], "spl_set_id": ["61207a91-8b3c-4231-b98f-3cb9f4a4be09"], "manufacturer_name": ["Afaxys Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 CARTON (50102-220-23)  / 1 BLISTER PACK in 1 POUCH (50102-220-21)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "50102-220-23", "marketing_start_date": "20161114"}], "brand_name": "Aubra EQ", "product_id": "50102-220_168ba8ff-87c7-4c10-a48d-6fe29555a997", "dosage_form": "KIT", "product_ndc": "50102-220", "generic_name": "Levonorgestrel and Ethinyl Estradiol", "labeler_name": "Afaxys Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aubra EQ", "application_number": "ANDA206886", "marketing_category": "ANDA", "marketing_start_date": "20161114", "listing_expiration_date": "20261231"}