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United States · US · US:70771-1550_34685b34-d41c-4a8b-b6db-9cd17e4ced70
betamethasone dipropionate
Orange BookUNIISPLATC D07AC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerZydus Lifesciences Limited
CountryUS (United States)
ATC codeD07AC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1170771155011 TUBE in 1 CARTON (70771-1550-1) / 15 g in 1 TUBE
- ndc1170771155041 TUBE in 1 CARTON (70771-1550-4) / 45 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
826Y60901U
BETAMETHASONE DIPROPIONATE
RxCUI 19254
Orange Book
A214048
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": "70771-1550_34685b34-d41c-4a8b-b6db-9cd17e4ced70",
"productndc": "70771-1550",
"dosage_form": "OINTMENT",
"orange_book": {
"appl_no": "214048",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 0.05% BASE",
"product_no": "001",
"approval_date": "Jul 14, 2020"
}
],
"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": "ANDA214048",
"marketing_category": "ANDA",
"nonproprietary_name": "betamethasone dipropionate",
"start_marketing_date": "20200720",
"active_numerator_strength": ".5"
}Related drugs
Other records sharing ATC code D07AC01.
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