levonorgestrel and ethinyl estradiol
Generic: levonorgestrel and ethinyl estradiol
Labeler: naari pte limitedDrug Facts
Product Profile
Brand Name
levonorgestrel and ethinyl estradiol
Generic Name
levonorgestrel and ethinyl estradiol
Labeler
naari pte limited
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
79929-003
Product ID
79929-003_187b07d3-8d52-1dba-e063-6394a90aed64
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207033
Listing Expiration
2026-12-31
Marketing Start
2022-12-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
79929003
Hyphenated Format
79929-003
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
levonorgestrel and ethinyl estradiol (source: ndc)
Generic Name
levonorgestrel and ethinyl estradiol (source: ndc)
Application Number
ANDA207033 (source: ndc)
Resolved Composition
Strengths
- 0.15 mg/0.03 mg
Packaging
- 3 BLISTER PACK in 1 CARTON (79929-003-07) / 1 KIT 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": "187b07d3-8d52-1dba-e063-6394a90aed64", "openfda": {"rxcui": ["238019", "748797", "748878"], "spl_set_id": ["ea9f7216-0358-43a9-96eb-5dad694ae9b8"], "manufacturer_name": ["Naari Pte Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (79929-003-07) / 1 KIT in 1 BLISTER PACK", "package_ndc": "79929-003-07", "marketing_start_date": "20221231"}], "brand_name": "Levonorgestrel and Ethinyl Estradiol", "product_id": "79929-003_187b07d3-8d52-1dba-e063-6394a90aed64", "dosage_form": "KIT", "product_ndc": "79929-003", "generic_name": "Levonorgestrel and Ethinyl Estradiol", "labeler_name": "Naari Pte Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levonorgestrel and Ethinyl Estradiol", "application_number": "ANDA207033", "marketing_category": "ANDA", "marketing_start_date": "20221231", "listing_expiration_date": "20261231"}