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United States · US · US:45802-021_2957986c-340c-4ef1-b78d-08b119fa703b
Betamethasone Dipropionate
Orange BookUNIISPLATC D07AC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPadagis Israel Pharmaceuticals Ltd
CountryUS (United States)
ATC codeD07AC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11458020214656.2 g in 1 BOTTLE, PLASTIC (45802-021-46)
Annotations
UNII (FDA Substance ID)
826Y60901U
BETAMETHASONE DIPROPIONATE
RxCUI 19254
Orange Book
A072538
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": "45802-021_2957986c-340c-4ef1-b78d-08b119fa703b",
"productndc": "45802-021",
"dosage_form": "LOTION",
"orange_book": {
"appl_no": "072538",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 0.05% BASE",
"product_no": "001",
"approval_date": "Jan 31, 1990"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BETAMETHASONE DIPROPIONATE",
"proprietary_name": "Betamethasone Dipropionate",
"active_ingred_unit": "mg/g",
"application_number": "ANDA072538",
"marketing_category": "ANDA",
"nonproprietary_name": "Betamethasone Dipropionate",
"start_marketing_date": "20060630",
"active_numerator_strength": ".5"
}Related drugs
Other records sharing ATC code D07AC01.
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