phenylephrine hydrochloride
Generic: phenylephrine hydrochloride
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
phenylephrine hydrochloride
Generic Name
phenylephrine hydrochloride
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION
Routes
Active Ingredients
phenylephrine hydrochloride 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0641-6142
Product ID
0641-6142_f73e455e-cbfa-48af-b4ce-505de8e8f761
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA203826
Listing Expiration
2026-12-31
Marketing Start
2012-12-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06416142
Hyphenated Format
0641-6142
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
NDA203826 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 25 VIAL in 1 CARTON (0641-6142-25) / 1 mL in 1 VIAL (0641-6142-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f73e455e-cbfa-48af-b4ce-505de8e8f761", "openfda": {"unii": ["04JA59TNSJ"], "rxcui": ["1232651", "1666372", "2262018", "2634228", "2634233", "2634235"], "spl_set_id": ["e1a7ab4b-0afe-4463-a039-5be0323cf2f7"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0641-6142-25) / 1 mL in 1 VIAL (0641-6142-01)", "package_ndc": "0641-6142-25", "marketing_start_date": "20121218"}], "brand_name": "Phenylephrine Hydrochloride", "product_id": "0641-6142_f73e455e-cbfa-48af-b4ce-505de8e8f761", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0641-6142", "generic_name": "Phenylephrine Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenylephrine Hydrochloride", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "NDA203826", "marketing_category": "NDA", "marketing_start_date": "20121218", "listing_expiration_date": "20261231"}