portia

Generic: levonorgestrel and ethinyl estradiol

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name portia
Generic Name levonorgestrel and ethinyl estradiol
Labeler teva pharmaceuticals usa, inc.
Dosage Form KIT
Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0555-9020
Product ID 0555-9020_4d63fa4a-ff46-4f2e-b9d5-cab4f5fe1d85
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075866
Listing Expiration 2026-12-31
Marketing Start 2002-06-27

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05559020
Hyphenated Format 0555-9020

Supplemental Identifiers

RxCUI
238019 748797 748878 751890

Packaging Origin

Original Packager
true

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 portia (source: ndc)
Generic Name levonorgestrel and ethinyl estradiol (source: ndc)
Application Number ANDA075866 (source: ndc)

Resolved Composition

Strengths
  • 0.15 mg/0.03 mg
source: label
Packaging
  • 6 POUCH in 1 CARTON (0555-9020-58) / 1 BLISTER PACK in 1 POUCH (0555-9020-79) / 1 KIT in 1 BLISTER PACK
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": "4d63fa4a-ff46-4f2e-b9d5-cab4f5fe1d85", "openfda": {"rxcui": ["238019", "748797", "748878", "751890"], "spl_set_id": ["c78b236b-85c4-4258-a524-cea08775100c"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 POUCH in 1 CARTON (0555-9020-58)  / 1 BLISTER PACK in 1 POUCH (0555-9020-79)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "0555-9020-58", "marketing_start_date": "20020627"}], "brand_name": "Portia", "product_id": "0555-9020_4d63fa4a-ff46-4f2e-b9d5-cab4f5fe1d85", "dosage_form": "KIT", "product_ndc": "0555-9020", "generic_name": "Levonorgestrel and Ethinyl Estradiol", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Portia", "application_number": "ANDA075866", "marketing_category": "ANDA", "marketing_start_date": "20020627", "listing_expiration_date": "20261231"}