progesterone
Generic: progesterone
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
progesterone
Generic Name
progesterone
Labeler
preferred pharmaceuticals inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
progesterone 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8719
Product ID
68788-8719_669c35d3-43cd-48b6-b450-42fe5717f04b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200900
Listing Expiration
2026-12-31
Marketing Start
2024-07-26
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888719
Hyphenated Format
68788-8719
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA200900 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (68788-8719-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "669c35d3-43cd-48b6-b450-42fe5717f04b", "openfda": {"nui": ["M0017672", "N0000175601"], "unii": ["4G7DS2Q64Y"], "rxcui": ["312641"], "spl_set_id": ["41c9546c-a854-4395-9506-d1be61f4e60f"], "pharm_class_cs": ["Progesterone [CS]"], "pharm_class_epc": ["Progesterone [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68788-8719-3)", "package_ndc": "68788-8719-3", "marketing_start_date": "20240726"}], "brand_name": "PROGESTERONE", "product_id": "68788-8719_669c35d3-43cd-48b6-b450-42fe5717f04b", "dosage_form": "CAPSULE", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "68788-8719", "generic_name": "PROGESTERONE", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROGESTERONE", "active_ingredients": [{"name": "PROGESTERONE", "strength": "200 mg/1"}], "application_number": "ANDA200900", "marketing_category": "ANDA", "marketing_start_date": "20240726", "listing_expiration_date": "20261231"}