betamethasone dipropionate

Generic: betamethasone dipropionate

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name betamethasone dipropionate
Generic Name betamethasone dipropionate
Labeler sun pharmaceutical industries, inc.
Dosage Form CREAM, AUGMENTED
Routes
TOPICAL
Active Ingredients

betamethasone dipropionate .5 mg/g

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 51672-1310
Product ID 51672-1310_3fb723a8-70e1-d700-e063-6294a90a53c5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076543
Listing Expiration 2026-12-31
Marketing Start 2003-12-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516721310
Hyphenated Format 51672-1310

Supplemental Identifiers

RxCUI
848176
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 ANDA076543 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51672-1310-1) / 15 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1310-2) / 30 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51672-1310-3) / 50 g in 1 TUBE
source: ndc

Packages (3)

51672-1310-1 1 TUBE in 1 CARTON (51672-1310-1) / 15 g in 1 TUBE 51672-1310-2 1 TUBE in 1 CARTON (51672-1310-2) / 30 g in 1 TUBE 51672-1310-3 1 TUBE in 1 CARTON (51672-1310-3) / 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": "3fb723a8-70e1-d700-e063-6294a90a53c5", "openfda": {"unii": ["826Y60901U"], "rxcui": ["848176"], "spl_set_id": ["000ae256-a337-4903-845b-003777a4efa8"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1310-1)  / 15 g in 1 TUBE", "package_ndc": "51672-1310-1", "marketing_start_date": "20031209"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1310-2)  / 30 g in 1 TUBE", "package_ndc": "51672-1310-2", "marketing_start_date": "20031209"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1310-3)  / 50 g in 1 TUBE", "package_ndc": "51672-1310-3", "marketing_start_date": "20031209"}], "brand_name": "Betamethasone Dipropionate", "product_id": "51672-1310_3fb723a8-70e1-d700-e063-6294a90a53c5", "dosage_form": "CREAM, AUGMENTED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51672-1310", "generic_name": "Betamethasone Dipropionate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betamethasone Dipropionate", "active_ingredients": [{"name": "BETAMETHASONE DIPROPIONATE", "strength": ".5 mg/g"}], "application_number": "ANDA076543", "marketing_category": "ANDA", "marketing_start_date": "20031209", "listing_expiration_date": "20261231"}