nitroglycerin

Generic: nitroglycerin

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

Drug Facts

Product Profile

Brand Name nitroglycerin
Generic Name nitroglycerin
Labeler proficient rx lp
Dosage Form TABLET
Routes
SUBLINGUAL
Active Ingredients

nitroglycerin .4 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-225
Product ID 71205-225_8c1a4a70-9849-4cb2-9425-5cf5747d4fbc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208191
Listing Expiration 2026-12-31
Marketing Start 2016-08-29

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 71205225
Hyphenated Format 71205-225

Supplemental Identifiers

RxCUI
198039
UPC
0371205225254
UNII
G59M7S0WS3
NUI
N0000175415 M0014874 N0000009909

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 ANDA208191 (source: ndc)
Routes
SUBLINGUAL
source: ndc

Resolved Composition

Strengths
  • .4 mg/1
source: ndc
Packaging
  • 25 TABLET in 1 BOTTLE (71205-225-25)
  • 30 TABLET in 1 BOTTLE (71205-225-30)
  • 60 TABLET in 1 BOTTLE (71205-225-60)
  • 90 TABLET in 1 BOTTLE (71205-225-90)
source: ndc

Packages (4)

Ingredients (1)

nitroglycerin (.4 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBLINGUAL"], "spl_id": "8c1a4a70-9849-4cb2-9425-5cf5747d4fbc", "openfda": {"nui": ["N0000175415", "M0014874", "N0000009909"], "upc": ["0371205225254"], "unii": ["G59M7S0WS3"], "rxcui": ["198039"], "spl_set_id": ["67a15ee9-a6ae-4a60-8333-e06c608cfd71"], "pharm_class_cs": ["Nitrates [CS]"], "pharm_class_pe": ["Vasodilation [PE]"], "pharm_class_epc": ["Nitrate Vasodilator [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "25 TABLET in 1 BOTTLE (71205-225-25)", "package_ndc": "71205-225-25", "marketing_start_date": "20190201"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-225-30)", "package_ndc": "71205-225-30", "marketing_start_date": "20190201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-225-60)", "package_ndc": "71205-225-60", "marketing_start_date": "20190201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-225-90)", "package_ndc": "71205-225-90", "marketing_start_date": "20190201"}], "brand_name": "Nitroglycerin", "product_id": "71205-225_8c1a4a70-9849-4cb2-9425-5cf5747d4fbc", "dosage_form": "TABLET", "pharm_class": ["Nitrate Vasodilator [EPC]", "Nitrates [CS]", "Vasodilation [PE]"], "product_ndc": "71205-225", "generic_name": "Nitroglycerin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nitroglycerin", "active_ingredients": [{"name": "NITROGLYCERIN", "strength": ".4 mg/1"}], "application_number": "ANDA208191", "marketing_category": "ANDA", "marketing_start_date": "20160829", "listing_expiration_date": "20261231"}