Package 0904-7211-04

Brand: dantrolene sodium

Generic: dantrolene sodium
NDC Package

Package Facts

Identity

Package NDC 0904-7211-04
Digits Only 0904721104
Product NDC 0904-7211
Description

30 BLISTER PACK in 1 CARTON (0904-7211-04) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-06-20
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": "84d36630-2a5e-4020-820d-d2b8b53db9bb", "openfda": {"unii": ["287M0347EV"], "rxcui": ["856656"], "spl_set_id": ["90414d2f-7b2c-47f9-a096-2e7b7dd052de"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7211-04)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7211-04", "marketing_start_date": "20220620"}], "brand_name": "Dantrolene Sodium", "product_id": "0904-7211_84d36630-2a5e-4020-820d-d2b8b53db9bb", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Striated Muscle Contraction [PE]", "Decreased Striated Muscle Tone [PE]", "Skeletal Muscle Relaxant [EPC]"], "product_ndc": "0904-7211", "generic_name": "Dantrolene Sodium", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dantrolene Sodium", "active_ingredients": [{"name": "DANTROLENE SODIUM", "strength": "25 mg/1"}], "application_number": "ANDA076856", "marketing_category": "ANDA", "marketing_start_date": "20050301", "listing_expiration_date": "20261231"}