progesterone
Generic: progesterone
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
progesterone
Generic Name
progesterone
Labeler
proficient rx lp
Dosage Form
CAPSULE
Routes
Active Ingredients
progesterone 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-669
Product ID
71205-669_d9517fbd-a829-4218-a41e-d384cae5aa01
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205229
Listing Expiration
2026-12-31
Marketing Start
2021-01-08
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205669
Hyphenated Format
71205-669
Supplemental Identifiers
RxCUI
UPC
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
ANDA205229 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (71205-669-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d9517fbd-a829-4218-a41e-d384cae5aa01", "openfda": {"nui": ["M0017672", "N0000175601"], "upc": ["0371205669300"], "unii": ["4G7DS2Q64Y"], "rxcui": ["312641"], "spl_set_id": ["80a63b2b-96be-423d-abbd-13acc802f6da"], "pharm_class_cs": ["Progesterone [CS]"], "pharm_class_epc": ["Progesterone [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71205-669-30)", "package_ndc": "71205-669-30", "marketing_start_date": "20220614"}], "brand_name": "Progesterone", "product_id": "71205-669_d9517fbd-a829-4218-a41e-d384cae5aa01", "dosage_form": "CAPSULE", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "71205-669", "generic_name": "Progesterone", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Progesterone", "active_ingredients": [{"name": "PROGESTERONE", "strength": "200 mg/1"}], "application_number": "ANDA205229", "marketing_category": "ANDA", "marketing_start_date": "20210108", "listing_expiration_date": "20261231"}