nitroglycerin

Generic: nitroglycerin

Labeler: solaris pharma corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nitroglycerin
Generic Name nitroglycerin
Labeler solaris pharma corporation
Dosage Form OINTMENT
Routes
RECTAL
Active Ingredients

nitroglycerin 4 mg/g

Manufacturer
Solaris Pharma Corporation

Identifiers & Regulatory

Product NDC 73473-500
Product ID 73473-500_fa800efb-4cb4-44bf-9ec9-f35a32476022
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218756
Listing Expiration 2027-12-31
Marketing Start 2026-01-08

Pharmacologic Class

Established (EPC)
nitrate vasodilator [epc]
Chemical Structure
nitrates [cs]
Physiologic Effect
vasodilation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73473500
Hyphenated Format 73473-500

Supplemental Identifiers

RxCUI
1114466
UNII
G59M7S0WS3
NUI
N0000175415 M0014874 N0000009909

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 nitroglycerin (source: ndc)
Generic Name nitroglycerin (source: ndc)
Application Number ANDA218756 (source: ndc)
Routes
RECTAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/g
source: ndc
Packaging
  • 30 g in 1 TUBE (73473-500-30)
source: ndc

Packages (1)

73473-500-30 30 g in 1 TUBE (73473-500-30)

Ingredients (1)

nitroglycerin (4 mg/g)

Linked Drug Pages (1)

Nitroglycerin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RECTAL"], "spl_id": "fa800efb-4cb4-44bf-9ec9-f35a32476022", "openfda": {"nui": ["N0000175415", "M0014874", "N0000009909"], "unii": ["G59M7S0WS3"], "rxcui": ["1114466"], "spl_set_id": ["f0a76edb-9e63-4aa4-9362-7375c799b2b5"], "pharm_class_cs": ["Nitrates [CS]"], "pharm_class_pe": ["Vasodilation [PE]"], "pharm_class_epc": ["Nitrate Vasodilator [EPC]"], "manufacturer_name": ["Solaris Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 g in 1 TUBE (73473-500-30)", "package_ndc": "73473-500-30", "marketing_start_date": "20260108"}], "brand_name": "Nitroglycerin", "product_id": "73473-500_fa800efb-4cb4-44bf-9ec9-f35a32476022", "dosage_form": "OINTMENT", "pharm_class": ["Nitrate Vasodilator [EPC]", "Nitrates [CS]", "Vasodilation [PE]"], "product_ndc": "73473-500", "generic_name": "Nitroglycerin", "labeler_name": "Solaris Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nitroglycerin", "active_ingredients": [{"name": "NITROGLYCERIN", "strength": "4 mg/g"}], "application_number": "ANDA218756", "marketing_category": "ANDA", "marketing_start_date": "20260108", "listing_expiration_date": "20271231"}