Package 49884-362-01
Brand: dantrolene sodium
Generic: dantrolene sodiumPackage Facts
Identity
Package NDC
49884-362-01
Digits Only
4988436201
Product NDC
49884-362
Description
100 CAPSULE in 1 BOTTLE (49884-362-01)
Marketing
Marketing Status
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": "eaaa53d2-744b-4529-ad62-84ab6b4fdd51", "openfda": {"upc": ["0349884363017", "0349884364014"], "unii": ["287M0347EV"], "rxcui": ["856652", "856656", "856660"], "spl_set_id": ["11689f56-15e0-4350-b53f-ae96e5994fea"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (49884-362-01)", "package_ndc": "49884-362-01", "marketing_start_date": "20160328"}], "brand_name": "dantrolene sodium", "product_id": "49884-362_eaaa53d2-744b-4529-ad62-84ab6b4fdd51", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Striated Muscle Contraction [PE]", "Decreased Striated Muscle Tone [PE]", "Skeletal Muscle Relaxant [EPC]"], "product_ndc": "49884-362", "generic_name": "dantrolene sodium", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "dantrolene sodium", "active_ingredients": [{"name": "DANTROLENE SODIUM", "strength": "25 mg/1"}], "application_number": "NDA017443", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20160328", "listing_expiration_date": "20261231"}