progesterone
Generic: progesterone
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
progesterone
Generic Name
progesterone
Labeler
remedyrepack inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
progesterone 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4166
Product ID
70518-4166_3fb8473d-fe36-7387-e063-6294a90a350b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200900
Listing Expiration
2026-12-31
Marketing Start
2024-08-22
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184166
Hyphenated Format
70518-4166
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
- 100 mg/1
Packaging
- 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-4166-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3fb8473d-fe36-7387-e063-6294a90a350b", "openfda": {"nui": ["M0017672", "N0000175601"], "unii": ["4G7DS2Q64Y"], "rxcui": ["260243"], "spl_set_id": ["947ebb7c-492b-4b83-aa1c-81e282df6421"], "pharm_class_cs": ["Progesterone [CS]"], "pharm_class_epc": ["Progesterone [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-4166-0)", "package_ndc": "70518-4166-0", "marketing_start_date": "20240822"}], "brand_name": "PROGESTERONE", "product_id": "70518-4166_3fb8473d-fe36-7387-e063-6294a90a350b", "dosage_form": "CAPSULE", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "70518-4166", "generic_name": "PROGESTERONE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROGESTERONE", "active_ingredients": [{"name": "PROGESTERONE", "strength": "100 mg/1"}], "application_number": "ANDA200900", "marketing_category": "ANDA", "marketing_start_date": "20240822", "listing_expiration_date": "20261231"}