desogestrel and ethinyl estradiol

Generic: desogestrel and ethinyl estradiol

Labeler: apotex corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name desogestrel and ethinyl estradiol
Generic Name desogestrel and ethinyl estradiol
Labeler apotex corp.
Dosage Form KIT
Manufacturer
Apotex Corp.

Identifiers & Regulatory

Product NDC 60505-4896
Product ID 60505-4896_49718fe6-b8d0-6db9-e063-6294a90aa923
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207067
Listing Expiration 2027-12-31
Marketing Start 2026-02-05

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 605054896
Hyphenated Format 60505-4896

Supplemental Identifiers

RxCUI
240707 748797 749848

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 desogestrel and ethinyl estradiol (source: ndc)
Generic Name desogestrel and ethinyl estradiol (source: ndc)
Application Number ANDA207067 (source: ndc)

Resolved Composition

Strengths
  • 0.15 mg/0.03 mg
  • 0.15 mg
  • 0.03 mg
source: label
Packaging
  • 3 BLISTER PACK in 1 CARTON (60505-4896-1) / 1 KIT in 1 BLISTER PACK * 21 TABLET in 1 BLISTER PACK * 7 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "49718fe6-b8d0-6db9-e063-6294a90aa923", "openfda": {"rxcui": ["240707", "748797", "749848"], "spl_set_id": ["9bb13b85-5d54-4689-b915-50b1da3a525b"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (60505-4896-1)  / 1 KIT in 1 BLISTER PACK *  21 TABLET in 1 BLISTER PACK *  7 TABLET in 1 BLISTER PACK", "package_ndc": "60505-4896-1", "marketing_start_date": "20260205"}], "brand_name": "desogestrel and ethinyl estradiol", "product_id": "60505-4896_49718fe6-b8d0-6db9-e063-6294a90aa923", "dosage_form": "KIT", "product_ndc": "60505-4896", "generic_name": "desogestrel and ethinyl estradiol", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "desogestrel and ethinyl estradiol", "application_number": "ANDA207067", "marketing_category": "ANDA", "marketing_start_date": "20260205", "listing_expiration_date": "20271231"}