Package 64850-841-01

Brand: dantrolene sodium

Generic: dantrolene sodium
NDC Package

Package Facts

Identity

Package NDC 64850-841-01
Digits Only 6485084101
Product NDC 64850-841
Description

100 CAPSULE in 1 BOTTLE (64850-841-01)

Marketing

Marketing Status
Marketed Since 2005-10-26
Brand dantrolene sodium
Generic dantrolene sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e3fc6ec6-cdde-456a-81bd-8ebd07065afc", "openfda": {"upc": ["0364850842013", "0364850840019", "0364850841016"], "unii": ["287M0347EV"], "rxcui": ["856652", "856656", "856660"], "spl_set_id": ["e637fb20-6a17-4522-810a-990bf1409732"], "manufacturer_name": ["Elite Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (64850-841-01)", "package_ndc": "64850-841-01", "marketing_start_date": "20051026"}], "brand_name": "Dantrolene Sodium", "product_id": "64850-841_e3fc6ec6-cdde-456a-81bd-8ebd07065afc", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Striated Muscle Contraction [PE]", "Decreased Striated Muscle Tone [PE]", "Skeletal Muscle Relaxant [EPC]"], "product_ndc": "64850-841", "generic_name": "dantrolene sodium", "labeler_name": "Elite Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dantrolene Sodium", "active_ingredients": [{"name": "DANTROLENE SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA076686", "marketing_category": "ANDA", "marketing_start_date": "20051026", "listing_expiration_date": "20261231"}