dexamethasone

Generic: dexamethasone

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dexamethasone
Generic Name dexamethasone
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dexamethasone 4 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-703
Product ID 71205-703_6f917c55-034a-40c5-9011-0e10e94d0eba
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA088481
Listing Expiration 2026-12-31
Marketing Start 2021-06-28

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205703
Hyphenated Format 71205-703

Supplemental Identifiers

RxCUI
197582
UPC
0371205703202
UNII
7S5I7G3JQL
NUI
N0000175576 N0000175450

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 dexamethasone (source: ndc)
Generic Name dexamethasone (source: ndc)
Application Number ANDA088481 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (71205-703-20)
  • 30 TABLET in 1 BOTTLE (71205-703-30)
  • 60 TABLET in 1 BOTTLE (71205-703-60)
  • 90 TABLET in 1 BOTTLE (71205-703-90)
source: ndc

Packages (4)

Ingredients (1)

dexamethasone (4 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6f917c55-034a-40c5-9011-0e10e94d0eba", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0371205703202"], "unii": ["7S5I7G3JQL"], "rxcui": ["197582"], "spl_set_id": ["6f917c55-034a-40c5-9011-0e10e94d0eba"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (71205-703-20)", "package_ndc": "71205-703-20", "marketing_start_date": "20221004"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-703-30)", "package_ndc": "71205-703-30", "marketing_start_date": "20221004"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-703-60)", "package_ndc": "71205-703-60", "marketing_start_date": "20221004"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-703-90)", "package_ndc": "71205-703-90", "marketing_start_date": "20221004"}], "brand_name": "Dexamethasone", "product_id": "71205-703_6f917c55-034a-40c5-9011-0e10e94d0eba", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "71205-703", "generic_name": "dexamethasone", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": "4 mg/1"}], "application_number": "ANDA088481", "marketing_category": "ANDA", "marketing_start_date": "20210628", "listing_expiration_date": "20261231"}