norethindrone and ethinyl estradiol
Generic: norethindrone and ethinyl estradiol
Labeler: naari pte limitedDrug Facts
Product Profile
Brand Name
norethindrone and ethinyl estradiol
Generic Name
norethindrone and ethinyl estradiol
Labeler
naari pte limited
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
79929-007
Product ID
79929-007_16aaf795-d54a-9f9c-e063-6394a90a09c4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206864
Listing Expiration
2026-12-31
Marketing Start
2022-12-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
79929007
Hyphenated Format
79929-007
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
norethindrone and ethinyl estradiol (source: ndc)
Generic Name
norethindrone and ethinyl estradiol (source: ndc)
Application Number
ANDA206864 (source: ndc)
Resolved Composition
Strengths
- 1 mg/0.035 mg
- 1 mg
- 0.035 mg
Packaging
- 3 BLISTER PACK in 1 CARTON (79929-007-07) / 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": "16aaf795-d54a-9f9c-e063-6394a90a09c4", "openfda": {"rxcui": ["312033", "748797", "749858"], "spl_set_id": ["9bd9119e-a874-41e2-ac58-b7f0d155d2fb"], "manufacturer_name": ["Naari Pte Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (79929-007-07) / 1 KIT in 1 BLISTER PACK", "package_ndc": "79929-007-07", "marketing_start_date": "20221231"}], "brand_name": "Norethindrone and ethinyl estradiol", "product_id": "79929-007_16aaf795-d54a-9f9c-e063-6394a90a09c4", "dosage_form": "KIT", "product_ndc": "79929-007", "generic_name": "Norethindrone and ethinyl estradiol", "labeler_name": "Naari Pte Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norethindrone and ethinyl estradiol", "application_number": "ANDA206864", "marketing_category": "ANDA", "marketing_start_date": "20221231", "listing_expiration_date": "20261231"}