betamethasone dipropionate
Generic: betamethasone dipropionate
Labeler: zydus lifesciences limitedDrug Facts
Product Profile
Brand Name
betamethasone dipropionate
Generic Name
betamethasone dipropionate
Labeler
zydus lifesciences limited
Dosage Form
OINTMENT
Routes
Active Ingredients
betamethasone dipropionate .5 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
70771-1550
Product ID
70771-1550_34685b34-d41c-4a8b-b6db-9cd17e4ced70
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214048
Listing Expiration
2026-12-31
Marketing Start
2020-07-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
707711550
Hyphenated Format
70771-1550
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
betamethasone dipropionate (source: ndc)
Generic Name
betamethasone dipropionate (source: ndc)
Application Number
ANDA214048 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/g
Packaging
- 1 TUBE in 1 CARTON (70771-1550-1) / 15 g in 1 TUBE
- 1 TUBE in 1 CARTON (70771-1550-4) / 45 g in 1 TUBE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "34685b34-d41c-4a8b-b6db-9cd17e4ced70", "openfda": {"unii": ["826Y60901U"], "rxcui": ["197405"], "spl_set_id": ["f531da27-2435-49a3-8992-c65240c6a7fe"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (70771-1550-1) / 15 g in 1 TUBE", "package_ndc": "70771-1550-1", "marketing_start_date": "20200720"}, {"sample": false, "description": "1 TUBE in 1 CARTON (70771-1550-4) / 45 g in 1 TUBE", "package_ndc": "70771-1550-4", "marketing_start_date": "20200720"}], "brand_name": "betamethasone dipropionate", "product_id": "70771-1550_34685b34-d41c-4a8b-b6db-9cd17e4ced70", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70771-1550", "generic_name": "betamethasone dipropionate", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "betamethasone dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA214048", "marketing_category": "ANDA", "marketing_start_date": "20200720", "listing_expiration_date": "20261231"}