tilia fe

Generic: ndac and ee tablets and ferrous fumarate tablets

Labeler: mayne pharma inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tilia fe
Generic Name ndac and ee tablets and ferrous fumarate tablets
Labeler mayne pharma inc.
Dosage Form KIT
Manufacturer
Mayne Pharma Inc.

Identifiers & Regulatory

Product NDC 51862-896
Product ID 51862-896_3cb85cc7-db23-4b6e-b5a1-e25c589994c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202962
Listing Expiration 2026-12-31
Marketing Start 2020-10-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51862896
Hyphenated Format 51862-896

Supplemental Identifiers

RxCUI
259176 1358762 1359130 1359131 1359132 1359134

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 tilia fe (source: ndc)
Generic Name ndac and ee tablets and ferrous fumarate tablets (source: ndc)
Application Number ANDA202962 (source: ndc)

Resolved Composition

Strengths
  • 1 mg
  • 20 mcg
  • 30 mcg
  • 35 mcg
  • 75 mg
source: label
Packaging
  • 1 BLISTER PACK in 1 PACKET (51862-896-01) / 1 KIT in 1 BLISTER PACK
  • 1 BLISTER PACK in 1 CARTON (51862-896-02) / 1 KIT in 1 BLISTER PACK
  • 6 BLISTER PACK in 1 CARTON (51862-896-06) / 1 KIT in 1 BLISTER PACK
source: ndc

Packages (3)

51862-896-01 1 BLISTER PACK in 1 PACKET (51862-896-01) / 1 KIT in 1 BLISTER PACK 51862-896-02 1 BLISTER PACK in 1 CARTON (51862-896-02) / 1 KIT in 1 BLISTER PACK 51862-896-06 6 BLISTER PACK in 1 CARTON (51862-896-06) / 1 KIT in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Tilia Fe ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "3cb85cc7-db23-4b6e-b5a1-e25c589994c9", "openfda": {"rxcui": ["259176", "1358762", "1359130", "1359131", "1359132", "1359134"], "spl_set_id": ["cebfb589-1b34-4f51-a0c8-c2c0cf4c7145"], "manufacturer_name": ["Mayne Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 PACKET (51862-896-01)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "51862-896-01", "marketing_start_date": "20201015"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (51862-896-02)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "51862-896-02", "marketing_start_date": "20201015"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (51862-896-06)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "51862-896-06", "marketing_start_date": "20201015"}], "brand_name": "Tilia Fe", "product_id": "51862-896_3cb85cc7-db23-4b6e-b5a1-e25c589994c9", "dosage_form": "KIT", "product_ndc": "51862-896", "generic_name": "NdAc and EE Tablets and Ferrous Fumarate Tablets", "labeler_name": "Mayne Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tilia Fe", "application_number": "ANDA202962", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}