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United States · US · US:68071-3669_209ca50a-3b5e-3799-e063-6294a90a80e4
Imipramine Hydrochloride
Orange BookUNIISPLATC N06AA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNuCare Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeN06AA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11680713669990 TABLET in 1 BOTTLE (68071-3669-9)
Annotations
UNII (FDA Substance ID)
BKE5Q1J60U
IMIPRAMINE HYDROCHLORIDE
RxCUI 150816
Orange Book
A040751
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "BKE5Q1J60U",
"rxcui": "150816",
"inchikey": "XZZXIYZZBJDEEP-UHFFFAOYSA-N",
"display_name": "IMIPRAMINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"02c19a0a-3d9d-4881-ad14-1687aafd87b5": {
"match": "brand_token",
"title": "IMIPRAMINE HYDROCHLORIDE TABLET [REMEDYREPACK INC.]",
"spl_version": "5",
"published_date": "2026-04-14"
}
},
"productid": "68071-3669_209ca50a-3b5e-3799-e063-6294a90a80e4",
"productndc": "68071-3669",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "040751",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG",
"product_no": "001",
"approval_date": "Feb 28, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "002",
"approval_date": "Feb 28, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "003",
"approval_date": "Feb 28, 2008"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "IMIPRAMINE HYDROCHLORIDE",
"proprietary_name": "Imipramine Hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA040751",
"marketing_category": "ANDA",
"nonproprietary_name": "Imipramine Hydrochloride",
"start_marketing_date": "20200801",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code N06AA02.
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