progesterone
Generic: progesterone
Labeler: bionpharma inc.Drug Facts
Product Profile
Brand Name
progesterone
Generic Name
progesterone
Labeler
bionpharma inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
progesterone 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69452-234
Product ID
69452-234_3e777dbd-754b-9d2e-e063-6294a90a42a6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200900
Listing Expiration
2026-12-31
Marketing Start
2018-11-28
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69452234
Hyphenated Format
69452-234
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
progesterone (source: ndc)
Generic Name
progesterone (source: ndc)
Application Number
ANDA200900 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (69452-234-20)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e777dbd-754b-9d2e-e063-6294a90a42a6", "openfda": {"nui": ["M0017672", "N0000175601"], "upc": ["0369452234204", "0369452233207"], "unii": ["4G7DS2Q64Y"], "rxcui": ["260243", "312641"], "spl_set_id": ["41b3c3a7-5fb8-4451-a96c-2bd02613c021"], "pharm_class_cs": ["Progesterone [CS]"], "pharm_class_epc": ["Progesterone [EPC]"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (69452-234-20)", "package_ndc": "69452-234-20", "marketing_start_date": "20181128"}], "brand_name": "PROGESTERONE", "product_id": "69452-234_3e777dbd-754b-9d2e-e063-6294a90a42a6", "dosage_form": "CAPSULE", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "69452-234", "generic_name": "PROGESTERONE", "labeler_name": "Bionpharma 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": "20181128", "listing_expiration_date": "20261231"}