Package 0781-3422-92

Brand: phenylephrine hydrochloride

Generic: phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0781-3422-92
Digits Only 0781342292
Product NDC 0781-3422
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3422-92) / 1 mL in 1 VIAL, SINGLE-DOSE (0781-3422-71)

Marketing

Marketing Status
Marketed Since 2019-12-16
Brand phenylephrine hydrochloride
Generic phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "14eec16d-4652-44a3-8cd3-a37b4280deb8", "openfda": {"unii": ["04JA59TNSJ"], "rxcui": ["1232651", "1666372"], "spl_set_id": ["6feb2da2-05ef-47bb-9d8d-01b81ad69059"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3422-92)  / 1 mL in 1 VIAL, SINGLE-DOSE (0781-3422-71)", "package_ndc": "0781-3422-92", "marketing_start_date": "20191216"}], "brand_name": "Phenylephrine Hydrochloride", "product_id": "0781-3422_14eec16d-4652-44a3-8cd3-a37b4280deb8", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0781-3422", "generic_name": "Phenylephrine Hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenylephrine Hydrochloride", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA208905", "marketing_category": "ANDA", "marketing_start_date": "20190905", "listing_expiration_date": "20261231"}