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 200 mg/1

Manufacturer
Direct Rx

Identifiers & Regulatory

Product NDC 72189-347
Product ID 72189-347_2c4c6aca-4b89-7f9f-e063-6394a90a0a23
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205229
Listing Expiration 2026-12-31
Marketing Start 2022-04-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189347
Hyphenated Format 72189-347

Supplemental Identifiers

RxCUI
312641
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
  • 200 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE (72189-347-90)
source: ndc

Packages (1)

72189-347-90 90 CAPSULE in 1 BOTTLE (72189-347-90)

Ingredients (1)

progesterone (200 mg/1)

Linked Drug Pages (1)

PROGESTERONE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4c6aca-4b89-7f9f-e063-6394a90a0a23", "openfda": {"nui": ["M0017672", "N0000175601"], "unii": ["4G7DS2Q64Y"], "rxcui": ["312641"], "spl_set_id": ["dc9e2088-e11e-7d32-e053-2a95a90a2995"], "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 (72189-347-90)", "package_ndc": "72189-347-90", "marketing_start_date": "20220414"}], "brand_name": "PROGESTERONE", "product_id": "72189-347_2c4c6aca-4b89-7f9f-e063-6394a90a0a23", "dosage_form": "CAPSULE", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "72189-347", "generic_name": "PROGESTERONE", "labeler_name": "Direct Rx", "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": "20220414", "listing_expiration_date": "20261231"}