jolessa
Generic: levonorgestrel / ethinyl estradiol
Labeler: teva pharmaceuticals usa, inc.Drug Facts
Product Profile
Brand Name
jolessa
Generic Name
levonorgestrel / ethinyl estradiol
Labeler
teva pharmaceuticals usa, inc.
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
0555-9123
Product ID
0555-9123_aaf5797d-3069-42ba-a8d2-088e5cd33b2c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA021544
Listing Expiration
2026-12-31
Marketing Start
2003-10-13
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05559123
Hyphenated Format
0555-9123
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
jolessa (source: ndc)
Generic Name
levonorgestrel / ethinyl estradiol (source: ndc)
Application Number
NDA021544 (source: ndc)
Resolved Composition
Strengths
- 0.15 mg
- 0.03 mg
Packaging
- 3 POUCH in 1 CARTON (0555-9123-66) / 1 BLISTER PACK in 1 POUCH / 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": "aaf5797d-3069-42ba-a8d2-088e5cd33b2c", "openfda": {"rxcui": ["238019", "748797", "751901", "762663"], "spl_set_id": ["f1076019-6f2c-4c90-9f3c-ab0c7cdd9315"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 CARTON (0555-9123-66) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK", "package_ndc": "0555-9123-66", "marketing_start_date": "20031013"}], "brand_name": "Jolessa", "product_id": "0555-9123_aaf5797d-3069-42ba-a8d2-088e5cd33b2c", "dosage_form": "KIT", "product_ndc": "0555-9123", "generic_name": "Levonorgestrel / Ethinyl Estradiol", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Jolessa", "application_number": "NDA021544", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20031013", "listing_expiration_date": "20261231"}