levonorgestrel and ethinyl estradiol

Generic: levonorgestrel and ethinyl estradiol

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

Drug Facts

Product Profile

Brand Name levonorgestrel and ethinyl estradiol
Generic Name levonorgestrel and ethinyl estradiol
Labeler lupin pharmaceuticals, inc.
Dosage Form KIT
Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-843
Product ID 68180-843_21d90467-0daa-44ee-8cad-f8a684cfa569
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091440
Listing Expiration 2026-12-31
Marketing Start 2012-10-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68180843
Hyphenated Format 68180-843

Supplemental Identifiers

RxCUI
238019 748797 751901

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 levonorgestrel and ethinyl estradiol (source: ndc)
Generic Name levonorgestrel and ethinyl estradiol (source: ndc)
Application Number ANDA091440 (source: ndc)

Resolved Composition

Strengths
  • 0.15 mg
  • 0.03 mg
  • 0.15 mg/0.03 mg
source: label
Packaging
  • 3 BLISTER PACK in 1 CARTON (68180-843-13) / 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": "21d90467-0daa-44ee-8cad-f8a684cfa569", "openfda": {"rxcui": ["238019", "748797", "751901"], "spl_set_id": ["58e85e02-93e7-42ba-b8f5-a36290c68423"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (68180-843-13)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "68180-843-13", "marketing_start_date": "20121024"}], "brand_name": "Levonorgestrel and Ethinyl Estradiol", "product_id": "68180-843_21d90467-0daa-44ee-8cad-f8a684cfa569", "dosage_form": "KIT", "product_ndc": "68180-843", "generic_name": "Levonorgestrel and Ethinyl Estradiol", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levonorgestrel and Ethinyl Estradiol", "application_number": "ANDA091440", "marketing_category": "ANDA", "marketing_start_date": "20121024", "listing_expiration_date": "20261231"}