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United States · US · US:0093-8305_e1f40596-aa5b-46a4-b2aa-add1150ac3a1
Cimetidine
Orange BookUNIISPLATC A02BA51
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTeva Pharmaceuticals USA, Inc.
CountryUS (United States)
ATC codeA02BA51
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110093830501100 TABLET, FILM COATED in 1 BOTTLE (0093-8305-01)
Annotations
UNII (FDA Substance ID)
80061L1WGD
CIMETIDINE
RxCUI 2541
Orange Book
A074463
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "80061L1WGD",
"rxcui": "2541",
"inchikey": "AQIXAKUUQRKLND-UHFFFAOYSA-N",
"display_name": "CIMETIDINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"0ab5ea2b-bd2f-49ec-9e92-033bed998797": {
"match": "brand_token",
"title": "CIMETIDINE TABLET, FILM COATED [BRYANT RANCH PREPACK]",
"spl_version": "1008",
"published_date": "2026-03-10"
}
},
"productid": "0093-8305_e1f40596-aa5b-46a4-b2aa-add1150ac3a1",
"productndc": "0093-8305",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "074463",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "800MG",
"product_no": "001",
"approval_date": "May 17, 1994"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CIMETIDINE",
"proprietary_name": "Cimetidine",
"active_ingred_unit": "mg/1",
"application_number": "ANDA074463",
"marketing_category": "ANDA",
"nonproprietary_name": "Cimetidine",
"start_marketing_date": "20031206",
"active_numerator_strength": "800"
}Related drugs
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