tydemy

Generic: drospirenone, ethinyl estradiol and levomefolate calcium and levomefolate calcium

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

Drug Facts

Product Profile

Brand Name tydemy
Generic Name drospirenone, ethinyl estradiol and levomefolate calcium and levomefolate calcium
Labeler lupin pharmaceuticals, inc.
Dosage Form KIT
Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-904
Product ID 68180-904_9229c82f-e84e-4805-90d2-a77e0fad63b5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205948
Listing Expiration 2026-12-31
Marketing Start 2020-11-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68180904
Hyphenated Format 68180-904

Supplemental Identifiers

RxCUI
1013628 1050492 1050493 1999724
UPC
0368180904717

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 tydemy (source: ndc)
Generic Name drospirenone, ethinyl estradiol and levomefolate calcium and levomefolate calcium (source: ndc)
Application Number ANDA205948 (source: ndc)

Resolved Composition

Strengths
  • 3 mg
  • 0.03 mg
  • 0.451 mg
source: label
Packaging
  • 3 POUCH in 1 CARTON (68180-904-73) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK * 21 TABLET, FILM COATED in 1 BLISTER PACK (68180-905-74) * 7 TABLET, FILM COATED in 1 BLISTER PACK (68180-910-74)
source: ndc

Packages (1)

68180-904-73 3 POUCH in 1 CARTON (68180-904-73) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK * 21 TABLET, FILM COATED in 1 BLISTER PACK (68180-905-74) * 7 TABLET, FILM COATED in 1 BLISTER PACK (68180-910-74)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Tydemy ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "9229c82f-e84e-4805-90d2-a77e0fad63b5", "openfda": {"upc": ["0368180904717"], "rxcui": ["1013628", "1050492", "1050493", "1999724"], "spl_set_id": ["e4766132-4faa-4f76-89fe-75d4a6fd737b"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 CARTON (68180-904-73)  / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK *  21 TABLET, FILM COATED in 1 BLISTER PACK (68180-905-74)  *  7 TABLET, FILM COATED in 1 BLISTER PACK (68180-910-74)", "package_ndc": "68180-904-73", "marketing_start_date": "20201120"}], "brand_name": "Tydemy", "product_id": "68180-904_9229c82f-e84e-4805-90d2-a77e0fad63b5", "dosage_form": "KIT", "product_ndc": "68180-904", "generic_name": "Drospirenone, Ethinyl Estradiol and Levomefolate Calcium and Levomefolate Calcium", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tydemy", "application_number": "ANDA205948", "marketing_category": "ANDA", "marketing_start_date": "20201120", "listing_expiration_date": "20261231"}