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United States · US · US:0143-9363_d0e3d92d-d96e-4d5e-98ca-3d18a4bc82d8
Labetalol HCl in Sodium Chloride
Orange BookUNIISPLATC C07AG01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHikma Pharmaceuticals USA Inc.
CountryUS (United States)
ATC codeC07AG01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11014393631010 BAG in 1 BOX (0143-9363-10) / 100 mL in 1 BAG (0143-9363-01)
Annotations
UNII (FDA Substance ID)
1GEV3BAW9J
LABETALOL HYDROCHLORIDE
RxCUI 202693
Orange Book
N213330
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "1GEV3BAW9J",
"rxcui": "202693",
"inchikey": "WQVZLXWQESQGIF-UHFFFAOYSA-N",
"display_name": "LABETALOL HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"d3ca153c-25b2-4506-91bd-bf9d6a4c01fe": {
"match": "brand_token",
"title": "LABETALOL HYDROCHLORIDE TABLET, FILM COATED [CARDINAL HEALTH 107, LLC]",
"spl_version": "4",
"published_date": "2026-06-01"
}
},
"productid": "0143-9363_d0e3d92d-d96e-4d5e-98ca-3d18a4bc82d8",
"productndc": "0143-9363",
"dosage_form": "INJECTION",
"orange_book": {
"appl_no": "213330",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "200MG/200ML (1MG/ML)",
"product_no": "001",
"approval_date": "Nov 9, 2020"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "100MG/100ML (1MG/ML)",
"product_no": "002",
"approval_date": "Nov 9, 2020"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "200MG/200ML (1MG/ML)",
"product_no": "003",
"approval_date": "Nov 9, 2020"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "300MG/300ML (1MG/ML)",
"product_no": "004",
"approval_date": "Nov 9, 2020"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "10MG/2ML (5MG/ML)",
"product_no": "005",
"approval_date": "Mar 18, 2022"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "20MG/4ML (5MG/ML)",
"product_no": "006",
"approval_date": "Aug 19, 2024"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "LABETALOL HYDROCHLORIDE",
"proprietary_name": "Labetalol HCl in Sodium Chloride",
"active_ingred_unit": "mg/mL",
"application_number": "NDA213330",
"marketing_category": "NDA",
"nonproprietary_name": "LABETALOL HYDROCHLORIDE",
"start_marketing_date": "20201109",
"active_numerator_strength": "1"
}Related drugs
Other records sharing ATC code C07AG01.
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