progesterone

Generic: progesterone

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name progesterone
Generic Name progesterone
Labeler direct_rx
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

progesterone 100 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-654
Product ID 72189-654_462ae686-7265-4852-e063-6294a90aae98
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205229
Listing Expiration 2026-12-31
Marketing Start 2025-12-17

Pharmacologic Class

Established (EPC)
progesterone [epc]
Chemical Structure
progesterone [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189654
Hyphenated Format 72189-654

Supplemental Identifiers

RxCUI
260243
UNII
4G7DS2Q64Y
NUI
M0017672 N0000175601

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE (72189-654-90)
source: ndc

Packages (1)

Ingredients (1)

progesterone (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "462ae686-7265-4852-e063-6294a90aae98", "openfda": {"nui": ["M0017672", "N0000175601"], "unii": ["4G7DS2Q64Y"], "rxcui": ["260243"], "spl_set_id": ["462ae686-7264-4852-e063-6294a90aae98"], "pharm_class_cs": ["Progesterone [CS]"], "pharm_class_epc": ["Progesterone [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72189-654-90)", "package_ndc": "72189-654-90", "marketing_start_date": "20251217"}], "brand_name": "Progesterone", "product_id": "72189-654_462ae686-7265-4852-e063-6294a90aae98", "dosage_form": "CAPSULE", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "72189-654", "generic_name": "Progesterone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Progesterone", "active_ingredients": [{"name": "PROGESTERONE", "strength": "100 mg/1"}], "application_number": "ANDA205229", "marketing_category": "ANDA", "marketing_start_date": "20251217", "listing_expiration_date": "20261231"}