portia
Generic: levonorgestrel and ethinyl estradiol
Labeler: teva pharmaceuticals usa, inc.Drug Facts
Product Profile
Brand Name
portia
Generic Name
levonorgestrel and ethinyl estradiol
Labeler
teva pharmaceuticals usa, inc.
Dosage Form
KIT
Manufacturer
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
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
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
Packaging
- 6 POUCH in 1 CARTON (0555-9020-58) / 1 BLISTER PACK in 1 POUCH (0555-9020-79) / 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": "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"}