phenylephrine hydrochloride
Generic: phenylephrine hydrochloride
Labeler: sandoz incDrug Facts
Product Profile
Brand Name
phenylephrine hydrochloride
Generic Name
phenylephrine hydrochloride
Labeler
sandoz inc
Dosage Form
INJECTION
Routes
Active Ingredients
phenylephrine hydrochloride 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0781-9227
Product ID
0781-9227_eb4076c0-0b18-332f-e053-2a95a90aae13
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208905
Listing Expiration
2026-12-31
Marketing Start
2021-02-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07819227
Hyphenated Format
0781-9227
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
phenylephrine hydrochloride (source: ndc)
Generic Name
phenylephrine hydrochloride (source: ndc)
Application Number
ANDA208905 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0781-9227-95) / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE (0781-9227-75)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "eb4076c0-0b18-332f-e053-2a95a90aae13", "openfda": {"unii": ["04JA59TNSJ"], "rxcui": ["1232651", "1666372"], "spl_set_id": ["5788f8c6-f868-4b83-81dc-dc485d8716c0"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0781-9227-95) / 5 mL in 1 VIAL, PHARMACY BULK PACKAGE (0781-9227-75)", "package_ndc": "0781-9227-95", "marketing_start_date": "20210217"}], "brand_name": "Phenylephrine Hydrochloride", "product_id": "0781-9227_eb4076c0-0b18-332f-e053-2a95a90aae13", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0781-9227", "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": "20210217", "listing_expiration_date": "20261231"}