fludrocortisone acetate

Generic: fludrocortisone acetate

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fludrocortisone acetate
Generic Name fludrocortisone acetate
Labeler northstar rx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fludrocortisone acetate .1 mg/1

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 72603-170
Product ID 72603-170_04ad6ba3-6782-b5df-e063-6294a90a7e6e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215279
Listing Expiration 2026-12-31
Marketing Start 2023-09-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603170
Hyphenated Format 72603-170

Supplemental Identifiers

RxCUI
313979
UPC
0372603170016
UNII
V47IF0PVH4

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 fludrocortisone acetate (source: ndc)
Generic Name fludrocortisone acetate (source: ndc)
Application Number ANDA215279 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72603-170-01)
source: ndc

Packages (1)

72603-170-01 100 TABLET in 1 BOTTLE (72603-170-01)

Ingredients (1)

fludrocortisone acetate (.1 mg/1)

Linked Drug Pages (1)

Fludrocortisone Acetate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "04ad6ba3-6782-b5df-e063-6294a90a7e6e", "openfda": {"upc": ["0372603170016"], "unii": ["V47IF0PVH4"], "rxcui": ["313979"], "spl_set_id": ["04ad6ba3-6781-b5df-e063-6294a90a7e6e"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-170-01)", "package_ndc": "72603-170-01", "marketing_start_date": "20230907"}], "brand_name": "Fludrocortisone Acetate", "product_id": "72603-170_04ad6ba3-6782-b5df-e063-6294a90a7e6e", "dosage_form": "TABLET", "product_ndc": "72603-170", "generic_name": "Fludrocortisone Acetate", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fludrocortisone Acetate", "active_ingredients": [{"name": "FLUDROCORTISONE ACETATE", "strength": ".1 mg/1"}], "application_number": "ANDA215279", "marketing_category": "ANDA", "marketing_start_date": "20230907", "listing_expiration_date": "20261231"}