Package 70121-1388-8

Brand: dexmedetomidine hydrochloride

Generic: dexmedetomidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70121-1388-8
Digits Only 7012113888
Product NDC 70121-1388
Product ID 70121-1388_795f643f-855c-4ba4-9bad-a96334c1a2fb
Description

20 BOTTLE, GLASS in 1 CARTON (70121-1388-8) / 50 mL in 1 BOTTLE, GLASS (70121-1388-1)

Marketing

Marketing Status
Marketed Since 2020-05-20
Brand dexmedetomidine hydrochloride
Generic dexmedetomidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Dexmedetomidine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "795f643f-855c-4ba4-9bad-a96334c1a2fb", "openfda": {"upc": ["0370121138914", "0370121138815", "0370121138884"], "unii": ["1018WH7F9I"], "rxcui": ["1718906", "1718909"], "spl_set_id": ["eb1ba463-ab42-4f49-9ebe-3ad5af108326"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BOTTLE, GLASS in 1 CARTON (70121-1388-8)  / 50 mL in 1 BOTTLE, GLASS (70121-1388-1)", "package_ndc": "70121-1388-8", "marketing_start_date": "20200520"}], "brand_name": "Dexmedetomidine Hydrochloride", "product_id": "70121-1388_795f643f-855c-4ba4-9bad-a96334c1a2fb", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "70121-1388", "generic_name": "Dexmedetomidine Hydrochloride", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmedetomidine Hydrochloride", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "4 ug/mL"}], "application_number": "ANDA207551", "marketing_category": "ANDA", "marketing_start_date": "20200520", "listing_expiration_date": "20261231"}