nortrel 28 day

Generic: norethindrone and ethinyl estradiol

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nortrel 28 day
Generic Name norethindrone and ethinyl estradiol
Labeler a-s medication solutions
Dosage Form KIT
Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3229
Product ID 50090-3229_504c5166-e2ca-4a75-bb6a-02798584ca64
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072695
Listing Expiration 2026-12-31
Marketing Start 2001-06-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500903229
Hyphenated Format 50090-3229

Supplemental Identifiers

RxCUI
310463 748797 749879 751868

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 nortrel 28 day (source: ndc)
Generic Name norethindrone and ethinyl estradiol (source: ndc)
Application Number ANDA072695 (source: ndc)

Resolved Composition

Strengths
  • 1 mg/0.035 mg
  • 1 mg
  • 0.035 mg
  • 0.5 mg/0.035 mg
source: label
Packaging
  • 1 KIT in 1 KIT (50090-3229-0)
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": "504c5166-e2ca-4a75-bb6a-02798584ca64", "openfda": {"rxcui": ["310463", "748797", "749879", "751868"], "spl_set_id": ["33b895e4-b467-41b1-a812-8068cc5bb93e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (50090-3229-0)", "package_ndc": "50090-3229-0", "marketing_start_date": "20171030"}], "brand_name": "Nortrel 28 Day", "product_id": "50090-3229_504c5166-e2ca-4a75-bb6a-02798584ca64", "dosage_form": "KIT", "product_ndc": "50090-3229", "generic_name": "Norethindrone and Ethinyl Estradiol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortrel", "brand_name_suffix": "28 Day", "application_number": "ANDA072695", "marketing_category": "ANDA", "marketing_start_date": "20010606", "listing_expiration_date": "20261231"}