premarin vaginal
Generic: conjugated estrogens
Labeler: wyeth pharmaceuticals llc, a subsidiary of pfizer inc.Drug Facts
Product Profile
Brand Name
premarin vaginal
Generic Name
conjugated estrogens
Labeler
wyeth pharmaceuticals llc, a subsidiary of pfizer inc.
Dosage Form
CREAM
Routes
Active Ingredients
estrogens, conjugated .625 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
0046-0872
Product ID
0046-0872_94b7195e-3ce2-4e04-a814-9b63add4896e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA020216
Listing Expiration
2026-12-31
Marketing Start
1978-11-01
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00460872
Hyphenated Format
0046-0872
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
premarin vaginal (source: ndc)
Generic Name
conjugated estrogens (source: ndc)
Application Number
NDA020216 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .625 mg/g
Packaging
- 1 TUBE, WITH APPLICATOR in 1 CARTON (0046-0872-04) / 4 g in 1 TUBE, WITH APPLICATOR
- 1 TUBE, WITH APPLICATOR in 1 CARTON (0046-0872-21) / 30 g in 1 TUBE, WITH APPLICATOR
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["VAGINAL"], "spl_id": "94b7195e-3ce2-4e04-a814-9b63add4896e", "openfda": {"nui": ["N0000175825", "N0000000100", "M0007792"], "upc": ["0300460872217"], "unii": ["IU5QR144QX"], "rxcui": ["688240", "688242"], "spl_set_id": ["96609623-528e-4aba-cabe-7254aed816d5"], "pharm_class_cs": ["Estrogens, Conjugated (USP) [CS]"], "pharm_class_epc": ["Estrogen [EPC]"], "pharm_class_moa": ["Estrogen Receptor Agonists [MoA]"], "manufacturer_name": ["Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 CARTON (0046-0872-04) / 4 g in 1 TUBE, WITH APPLICATOR", "package_ndc": "0046-0872-04", "marketing_start_date": "19781101"}, {"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 CARTON (0046-0872-21) / 30 g in 1 TUBE, WITH APPLICATOR", "package_ndc": "0046-0872-21", "marketing_start_date": "19781101"}], "brand_name": "Premarin Vaginal", "product_id": "0046-0872_94b7195e-3ce2-4e04-a814-9b63add4896e", "dosage_form": "CREAM", "pharm_class": ["Estrogen Receptor Agonists [MoA]", "Estrogen [EPC]", "Estrogens", "Conjugated (USP) [CS]"], "product_ndc": "0046-0872", "generic_name": "conjugated estrogens", "labeler_name": "Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Premarin", "brand_name_suffix": "Vaginal", "active_ingredients": [{"name": "ESTROGENS, CONJUGATED", "strength": ".625 mg/g"}], "application_number": "NDA020216", "marketing_category": "NDA", "marketing_start_date": "19781101", "listing_expiration_date": "20261231"}