procardia xl

Generic: nifedipine

Labeler: pfizer laboratories div pfizer inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name procardia xl
Generic Name nifedipine
Labeler pfizer laboratories div pfizer inc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

nifedipine 90 mg/1

Manufacturer
Pfizer Laboratories Div Pfizer Inc

Identifiers & Regulatory

Product NDC 0069-2670
Product ID 0069-2670_c24a0478-46d4-413a-8d48-c21af0bc10e4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019684
Marketing Start 1989-09-06
Marketing End 2026-03-31

Pharmacologic Class

Established (EPC)
dihydropyridine calcium channel blocker [epc]
Mechanism of Action
calcium channel antagonists [moa]
Chemical Structure
dihydropyridines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00692670
Hyphenated Format 0069-2670

Supplemental Identifiers

RxCUI
207772 207773 207774 1812011 1812013 1812015
UNII
I9ZF7L6G2L
NUI
N0000000069 N0000175421 M0006414

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 procardia xl (source: ndc)
Generic Name nifedipine (source: ndc)
Application Number NDA019684 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 90 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2670-66)
source: ndc

Packages (1)

0069-2670-66 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2670-66)

Ingredients (1)

nifedipine (90 mg/1)

Linked Drug Pages (1)

Procardia XL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c24a0478-46d4-413a-8d48-c21af0bc10e4", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["207772", "207773", "207774", "1812011", "1812013", "1812015"], "spl_set_id": ["8ebcb33c-f43b-4b36-9f94-9774b2a59e06"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2670-66)", "package_ndc": "0069-2670-66", "marketing_end_date": "20260331", "marketing_start_date": "19890906"}], "brand_name": "Procardia XL", "product_id": "0069-2670_c24a0478-46d4-413a-8d48-c21af0bc10e4", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "0069-2670", "generic_name": "nifedipine", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Procardia", "brand_name_suffix": "XL", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "90 mg/1"}], "application_number": "NDA019684", "marketing_category": "NDA", "marketing_end_date": "20260331", "marketing_start_date": "19890906"}