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United States · US · US:39822-0151_02f79412-2198-a8af-e063-6394a90a0853
Liothyronine Sodium
Orange BookUNIISPLATC H03AA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerXGen Pharmaceuticals DJB, Inc.
CountryUS (United States)
ATC codeH03AA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1139822015111 VIAL in 1 CARTON (39822-0151-1) / 1 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
GCA9VV7D2N
LIOTHYRONINE SODIUM
RxCUI 142448
Orange Book
A076923
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "GCA9VV7D2N",
"rxcui": "142448",
"inchikey": "SBXXSUDPJJJJLC-YDALLXLXSA-M",
"display_name": "LIOTHYRONINE SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"57744c7c-af44-4bc4-a5a8-79f05710f469": {
"match": "brand_token",
"title": "LIOTHYRONINE SODIUM TABLET [PREFERRED PHARMACEUTICALS INC.]",
"spl_version": "8",
"published_date": "2026-05-25"
}
},
"productid": "39822-0151_02f79412-2198-a8af-e063-6394a90a0853",
"productndc": "39822-0151",
"dosage_form": "INJECTION, SOLUTION",
"orange_book": {
"appl_no": "076923",
"products": [
{
"rs": true,
"rld": false,
"te_code": null,
"strength": "EQ 0.01MG BASE/ML",
"product_no": "001",
"approval_date": "Aug 17, 2005"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LIOTHYRONINE SODIUM",
"proprietary_name": "Liothyronine Sodium",
"active_ingred_unit": "ug/mL",
"application_number": "ANDA076923",
"marketing_category": "ANDA",
"nonproprietary_name": "Liothyronine Sodium",
"start_marketing_date": "20050817",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code H03AA02.
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