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United States · US · US:0168-0055_3a499a57-9faa-419d-beeb-3aba6b8c2d7c
Betamethasone Dipropionate
Orange BookUNIISPLATC D07AC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerE. Fougera & Co. a division of Fougera Pharmaceuticals, LLC
CountryUS (United States)
ATC codeD07AC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1101680055151 TUBE in 1 CARTON (0168-0055-15) / 15 g in 1 TUBE
- ndc1101680055461 TUBE in 1 CARTON (0168-0055-46) / 45 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
826Y60901U
BETAMETHASONE DIPROPIONATE
RxCUI 19254
Orange Book
N019137
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "826Y60901U",
"rxcui": "19254",
"inchikey": "CIWBQSYVNNPZIQ-XYWKZLDCSA-N",
"display_name": "BETAMETHASONE DIPROPIONATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"b5291e39-40a0-4362-9281-97f5fb4025d9": {
"match": "brand_token",
"title": "BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED [A-S MEDICATION SOLUTIONS]",
"spl_version": "3",
"published_date": "2026-05-12"
}
},
"productid": "0168-0055_3a499a57-9faa-419d-beeb-3aba6b8c2d7c",
"productndc": "0168-0055",
"dosage_form": "CREAM",
"orange_book": {
"appl_no": "019137",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "EQ 0.05% BASE",
"product_no": "001",
"approval_date": "Jun 26, 1984"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BETAMETHASONE DIPROPIONATE",
"proprietary_name": "Betamethasone Dipropionate",
"active_ingred_unit": "mg/g",
"application_number": "NDA019137",
"marketing_category": "NDA",
"nonproprietary_name": "Betamethasone Dipropionate",
"start_marketing_date": "19840626",
"active_numerator_strength": ".5"
}Related drugs
Other records sharing ATC code D07AC01.
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