dexamethasone sodium phosphate

Generic: dexamethasone sodium phosphate

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dexamethasone sodium phosphate
Generic Name dexamethasone sodium phosphate
Labeler asclemed usa, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR INTRAVENOUS SOFT TISSUE
Active Ingredients

dexamethasone sodium phosphate 4 mg/mL

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-077
Product ID 76420-077_ead2db1e-54b5-fa3c-e053-2a95a90a1b97
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206781
Listing Expiration 2026-12-31
Marketing Start 2020-02-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420077
Hyphenated Format 76420-077

Supplemental Identifiers

RxCUI
1812194
UNII
AI9376Y64P

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 sodium phosphate (source: ndc)
Generic Name dexamethasone sodium phosphate (source: ndc)
Application Number ANDA206781 (source: ndc)
Routes
INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR INTRAVENOUS SOFT TISSUE
source: ndc

Resolved Composition

Strengths
  • 4 mg/mL
source: ndc
Packaging
  • 1 mL in 1 VIAL, SINGLE-DOSE (76420-077-01)
source: ndc

Packages (1)

76420-077-01 1 mL in 1 VIAL, SINGLE-DOSE (76420-077-01)

Ingredients (1)

dexamethasone sodium phosphate (4 mg/mL)

Linked Drug Pages (1)

DEXAMETHASONE SODIUM PHOSPHATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRA-ARTICULAR", "INTRALESIONAL", "INTRAMUSCULAR", "INTRAVENOUS", "SOFT TISSUE"], "spl_id": "ead2db1e-54b5-fa3c-e053-2a95a90a1b97", "openfda": {"unii": ["AI9376Y64P"], "rxcui": ["1812194"], "spl_set_id": ["ca762fbf-6bf5-4b39-8f40-3fb5f1f77778"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (76420-077-01)", "package_ndc": "76420-077-01", "marketing_start_date": "20200211"}], "brand_name": "DEXAMETHASONE SODIUM PHOSPHATE", "product_id": "76420-077_ead2db1e-54b5-fa3c-e053-2a95a90a1b97", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "76420-077", "generic_name": "DEXAMETHASONE SODIUM PHOSPHATE", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXAMETHASONE SODIUM PHOSPHATE", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "4 mg/mL"}], "application_number": "ANDA206781", "marketing_category": "ANDA", "marketing_start_date": "20200211", "listing_expiration_date": "20261231"}