nimodipine

Generic: nimodipine

Labeler: bionpharma inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nimodipine
Generic Name nimodipine
Labeler bionpharma inc.
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

nimodipine 30 mg/1

Manufacturer
BIONPHARMA INC.

Identifiers & Regulatory

Product NDC 69452-209
Product ID 69452-209_452704d5-dbeb-5833-e063-6394a90a1a9a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076740
Listing Expiration 2026-12-31
Marketing Start 2017-11-21

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 69452209
Hyphenated Format 69452-209

Supplemental Identifiers

RxCUI
198037
UNII
57WA9QZ5WH
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 nimodipine (source: ndc)
Generic Name nimodipine (source: ndc)
Application Number ANDA076740 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (69452-209-13) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
  • 10 BLISTER PACK in 1 CARTON (69452-209-20) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (2)

69452-209-13 3 BLISTER PACK in 1 CARTON (69452-209-13) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 69452-209-20 10 BLISTER PACK in 1 CARTON (69452-209-20) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Ingredients (1)

nimodipine (30 mg/1)

Linked Drug Pages (1)

Nimodipine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "452704d5-dbeb-5833-e063-6394a90a1a9a", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["57WA9QZ5WH"], "rxcui": ["198037"], "spl_set_id": ["e65d5108-22a2-4d87-a78d-15606f3cc9e2"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["BIONPHARMA INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (69452-209-13)  / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "69452-209-13", "marketing_start_date": "20171121"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (69452-209-20)  / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "69452-209-20", "marketing_start_date": "20171121"}], "brand_name": "Nimodipine", "product_id": "69452-209_452704d5-dbeb-5833-e063-6394a90a1a9a", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "69452-209", "generic_name": "Nimodipine", "labeler_name": "BIONPHARMA INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nimodipine", "active_ingredients": [{"name": "NIMODIPINE", "strength": "30 mg/1"}], "application_number": "ANDA076740", "marketing_category": "ANDA", "marketing_start_date": "20171121", "listing_expiration_date": "20261231"}