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United States · US · US:0075-0620_cdb74d6d-1a74-4156-a52a-710c55cb2927
Lovenox
Orange BookUNIISPLATC B01AB05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSanofi-Aventis U.S. LLC
CountryUS (United States)
ATC codeB01AB05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11007506204010 CELLO PACK in 1 CARTON (0075-0620-40) / 1 SYRINGE in 1 CELLO PACK (0075-0620-01) / .4 mL in 1 SYRINGE
Annotations
UNII (FDA Substance ID)
8NZ41MIK1O
ENOXAPARIN SODIUM
RxCUI 221095
Orange Book
N020164
APAPAPAPAPAPAP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "8NZ41MIK1O",
"rxcui": "221095",
"inchikey": null,
"display_name": "ENOXAPARIN SODIUM",
"substance_type": "polymer",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "SUBCUTANEOUS",
"spl_meta": {
"5017a927-2a24-4f27-89f9-27c805bf7d59": {
"match": "brand_token",
"title": "LOVENOX (ENOXAPARIN SODIUM) INJECTION [SANOFI-AVENTIS U.S. LLC]",
"spl_version": "33",
"published_date": "2026-05-29"
}
},
"productid": "0075-0620_cdb74d6d-1a74-4156-a52a-710c55cb2927",
"productndc": "0075-0620",
"dosage_form": "INJECTION",
"orange_book": {
"appl_no": "020164",
"products": [
{
"rs": false,
"rld": true,
"te_code": "AP",
"strength": "30MG/0.3ML (100MG/ML)",
"product_no": "001",
"approval_date": "Mar 29, 1993"
},
{
"rs": false,
"rld": true,
"te_code": "AP",
"strength": "40MG/0.4ML (100MG/ML)",
"product_no": "002",
"approval_date": "Jan 30, 1998"
},
{
"rs": false,
"rld": true,
"te_code": "AP",
"strength": "60MG/0.6ML (100MG/ML)",
"product_no": "003",
"approval_date": "Mar 27, 1998"
},
{
"rs": false,
"rld": true,
"te_code": "AP",
"strength": "80MG/0.8ML (100MG/ML)",
"product_no": "004",
"approval_date": "Mar 27, 1998"
},
{
"rs": true,
"rld": true,
"te_code": "AP",
"strength": "100MG/ML (100MG/ML)",
"product_no": "005",
"approval_date": "Mar 27, 1998"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "90MG/0.6ML (150MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
"product_no": "006",
"approval_date": "Jun 2, 2000"
},
{
"rs": false,
"rld": true,
"te_code": "AP",
"strength": "120MG/0.8ML (150MG/ML)",
"product_no": "007",
"approval_date": "Jun 2, 2000"
},
{
"rs": false,
"rld": true,
"te_code": "AP",
"strength": "150MG/ML (150MG/ML)",
"product_no": "008",
"approval_date": "Jun 2, 2000"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "300MG/3ML (100MG/ML)",
"product_no": "009",
"approval_date": "Jan 23, 2003"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ENOXAPARIN SODIUM",
"proprietary_name": "Lovenox",
"active_ingred_unit": "mg/.4mL",
"application_number": "NDA020164",
"marketing_category": "NDA",
"nonproprietary_name": "enoxaparin sodium",
"start_marketing_date": "19930329",
"active_numerator_strength": "40"
}Related drugs
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