azurette
Generic: desogestrel/ethinyl estradiol and ethinyl estradiol
Labeler: dr. reddys laboratories inc.Drug Facts
Product Profile
Brand Name
azurette
Generic Name
desogestrel/ethinyl estradiol and ethinyl estradiol
Labeler
dr. reddys laboratories inc.
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
75907-091
Product ID
75907-091_f64171dd-ac43-4be5-ba1d-51cbcff7991e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091247
Listing Expiration
2026-12-31
Marketing Start
2024-06-25
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
75907091
Hyphenated Format
75907-091
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
azurette (source: ndc)
Generic Name
desogestrel/ethinyl estradiol and ethinyl estradiol (source: ndc)
Application Number
ANDA091247 (source: ndc)
Resolved Composition
Strengths
- 0.15 mg
- 0.02 mg
- 0.01 mg
Packaging
- 1 BLISTER PACK in 1 PACKET (75907-091-28) / 1 KIT in 1 BLISTER PACK
- 6 BLISTER PACK in 1 CARTON (75907-091-62) / 1 KIT in 1 BLISTER PACK
Packages (2)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "f64171dd-ac43-4be5-ba1d-51cbcff7991e", "openfda": {"rxcui": ["248310", "249357", "748797", "759743", "831872"], "spl_set_id": ["f0288c8d-6ca0-41fa-93f2-b6c2d073891f"], "manufacturer_name": ["Dr. Reddys Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 PACKET (75907-091-28) / 1 KIT in 1 BLISTER PACK", "package_ndc": "75907-091-28", "marketing_start_date": "20240625"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (75907-091-62) / 1 KIT in 1 BLISTER PACK", "package_ndc": "75907-091-62", "marketing_start_date": "20240625"}], "brand_name": "Azurette", "product_id": "75907-091_f64171dd-ac43-4be5-ba1d-51cbcff7991e", "dosage_form": "KIT", "product_ndc": "75907-091", "generic_name": "desogestrel/ethinyl estradiol and ethinyl estradiol", "labeler_name": "Dr. Reddys Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azurette", "application_number": "ANDA091247", "marketing_category": "ANDA", "marketing_start_date": "20240625", "listing_expiration_date": "20261231"}