desogestrel and ethinyl estradiol
Generic: desogestrel and ethinyl estradiol
Labeler: apotex corp.Drug Facts
Product Profile
Brand Name
desogestrel and ethinyl estradiol
Generic Name
desogestrel and ethinyl estradiol
Labeler
apotex corp.
Dosage Form
KIT
Manufacturer
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
Packaging Origin
Original Packager
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
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
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"}