betamethasone dipropionate

Generic: betamethasone dipropionate

Labeler: lupin pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name betamethasone dipropionate
Generic Name betamethasone dipropionate
Labeler lupin pharmaceuticals, inc.
Dosage Form OINTMENT, AUGMENTED
Routes
TOPICAL
Active Ingredients

betamethasone dipropionate .5 mg/g

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-947
Product ID 68180-947_fb870496-75f5-4f2a-a156-2552d9c13e7f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209106
Listing Expiration 2027-12-31
Marketing Start 2020-03-19

Pharmacologic Class

Classes
corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68180947
Hyphenated Format 68180-947

Supplemental Identifiers

RxCUI
848180
UPC
0368180947028
UNII
826Y60901U

Packaging Origin

Original Packager
true

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 ANDA209106 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (68180-947-01) / 15 g in 1 TUBE
  • 1 TUBE in 1 CARTON (68180-947-02) / 50 g in 1 TUBE
source: ndc

Packages (2)

68180-947-01 1 TUBE in 1 CARTON (68180-947-01) / 15 g in 1 TUBE 68180-947-02 1 TUBE in 1 CARTON (68180-947-02) / 50 g in 1 TUBE

Ingredients (1)

betamethasone dipropionate (.5 mg/g)

Linked Drug Pages (1)

Betamethasone dipropionate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "fb870496-75f5-4f2a-a156-2552d9c13e7f", "openfda": {"upc": ["0368180947028"], "unii": ["826Y60901U"], "rxcui": ["848180"], "spl_set_id": ["216d5b7f-4236-4882-b899-be17cb1a1584"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68180-947-01)  / 15 g in 1 TUBE", "package_ndc": "68180-947-01", "marketing_start_date": "20200319"}, {"sample": false, "description": "1 TUBE in 1 CARTON (68180-947-02)  / 50 g in 1 TUBE", "package_ndc": "68180-947-02", "marketing_start_date": "20200319"}], "brand_name": "Betamethasone dipropionate", "product_id": "68180-947_fb870496-75f5-4f2a-a156-2552d9c13e7f", "dosage_form": "OINTMENT, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68180-947", "generic_name": "Betamethasone dipropionate", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA209106", "marketing_category": "ANDA", "marketing_start_date": "20200319", "listing_expiration_date": "20271231"}