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United States · US · US:51862-896_3cb85cc7-db23-4b6e-b5a1-e25c589994c9
Tilia Fe
Orange BookSPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMayne Pharma Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1151862896011 BLISTER PACK in 1 PACKET (51862-896-01) / 1 KIT in 1 BLISTER PACK
- ndc1151862896021 BLISTER PACK in 1 CARTON (51862-896-02) / 1 KIT in 1 BLISTER PACK
- ndc1151862896066 BLISTER PACK in 1 CARTON (51862-896-06) / 1 KIT in 1 BLISTER PACK
Annotations
Orange Book
A202962
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": null,
"spl_meta": {
"cebfb589-1b34-4f51-a0c8-c2c0cf4c7145": {
"match": "brand_token",
"title": "TILIA FE ( NDAC AND EE TABLETS AND FERROUS FUMARATE TABLETS ) KIT [MAYNE PHARMA INC.]",
"spl_version": "3",
"published_date": "2025-09-10"
}
},
"productid": "51862-896_3cb85cc7-db23-4b6e-b5a1-e25c589994c9",
"productndc": "51862-896",
"dosage_form": "KIT",
"orange_book": {
"appl_no": "202962",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "0.02MG,0.03MG,0.035MG;1MG,1MG,1MG",
"product_no": "001",
"approval_date": "Apr 15, 2020"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": null,
"proprietary_name": "Tilia Fe",
"active_ingred_unit": null,
"application_number": "ANDA202962",
"marketing_category": "ANDA",
"nonproprietary_name": "NdAc and EE Tablets and Ferrous Fumarate Tablets",
"start_marketing_date": "20201015",
"active_numerator_strength": null
}Access this data programmatically
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