Package 70700-157-01
Brand: midodrine hydrochloride
Generic: midodrine hydrochloridePackage Facts
Identity
Package NDC
70700-157-01
Digits Only
7070015701
Product NDC
70700-157
Description
100 TABLET in 1 BOTTLE, PLASTIC (70700-157-01)
Marketing
Marketing Status
Brand
midodrine hydrochloride
Generic
midodrine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2214523a-41b1-3644-6e7c-abc4f8b0b5cc", "openfda": {"upc": ["0370700157015", "0370700159019", "0370700158012"], "unii": ["59JV96YTXV"], "rxcui": ["993462", "993466", "993470"], "spl_set_id": ["a4332a41-2a0a-a14a-9ce5-1465f39ff725"], "manufacturer_name": ["Xiromed, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70700-157-01)", "package_ndc": "70700-157-01", "marketing_start_date": "20201015"}], "brand_name": "Midodrine Hydrochloride", "product_id": "70700-157_2214523a-41b1-3644-6e7c-abc4f8b0b5cc", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "70700-157", "generic_name": "midodrine hydrochloride", "labeler_name": "Xiromed, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midodrine Hydrochloride", "active_ingredients": [{"name": "MIDODRINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA207849", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}