nifedipine

Generic: nifedipine

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nifedipine
Generic Name nifedipine
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

nifedipine 30 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7642
Product ID 68788-7642_902d31db-8e45-4221-9308-2f02ea622a4c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210614
Listing Expiration 2026-12-31
Marketing Start 2020-02-28

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 687887642
Hyphenated Format 68788-7642

Supplemental Identifiers

RxCUI
1812011
UNII
I9ZF7L6G2L
NUI
N0000000069 N0000175421 M0006414

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 nifedipine (source: ndc)
Generic Name nifedipine (source: ndc)
Application Number ANDA210614 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-1)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-3)
  • 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-6)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-9)
source: ndc

Packages (4)

68788-7642-1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-1) 68788-7642-3 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-3) 68788-7642-6 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-6) 68788-7642-9 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-9)

Ingredients (1)

nifedipine (30 mg/1)

Linked Drug Pages (1)

Nifedipine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "902d31db-8e45-4221-9308-2f02ea622a4c", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011"], "spl_set_id": ["4ee466dc-5a4e-4c77-8e94-8b510cafd61b"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-1)", "package_ndc": "68788-7642-1", "marketing_start_date": "20200228"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-3)", "package_ndc": "68788-7642-3", "marketing_start_date": "20200228"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-6)", "package_ndc": "68788-7642-6", "marketing_start_date": "20200228"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-9)", "package_ndc": "68788-7642-9", "marketing_start_date": "20200228"}], "brand_name": "Nifedipine", "product_id": "68788-7642_902d31db-8e45-4221-9308-2f02ea622a4c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "68788-7642", "generic_name": "nifedipine", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA210614", "marketing_category": "ANDA", "marketing_start_date": "20200228", "listing_expiration_date": "20261231"}