progesterone
Generic: progesterone
Labeler: xiromed, llcDrug Facts
Product Profile
Brand Name
progesterone
Generic Name
progesterone
Labeler
xiromed, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
progesterone 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70700-286
Product ID
70700-286_0f25eef8-d21f-138d-dd9c-550b42f355dc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215634
Listing Expiration
2026-12-31
Marketing Start
2022-03-29
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70700286
Hyphenated Format
70700-286
Supplemental Identifiers
RxCUI
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
progesterone (source: ndc)
Generic Name
progesterone (source: ndc)
Application Number
ANDA215634 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 10 mL in 1 VIAL, MULTI-DOSE (70700-286-22)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "0f25eef8-d21f-138d-dd9c-550b42f355dc", "openfda": {"nui": ["M0017672", "N0000175601"], "unii": ["4G7DS2Q64Y"], "rxcui": ["312644"], "spl_set_id": ["dcfa4050-d142-b774-369f-8a421eb23c62"], "pharm_class_cs": ["Progesterone [CS]"], "pharm_class_epc": ["Progesterone [EPC]"], "manufacturer_name": ["XIROMED, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, MULTI-DOSE (70700-286-22)", "package_ndc": "70700-286-22", "marketing_start_date": "20220329"}], "brand_name": "PROGESTERONE", "product_id": "70700-286_0f25eef8-d21f-138d-dd9c-550b42f355dc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "70700-286", "generic_name": "PROGESTERONE", "labeler_name": "XIROMED, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROGESTERONE", "active_ingredients": [{"name": "PROGESTERONE", "strength": "50 mg/mL"}], "application_number": "ANDA215634", "marketing_category": "ANDA", "marketing_start_date": "20220329", "listing_expiration_date": "20261231"}