progesterone

Generic: progesterone

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name progesterone
Generic Name progesterone
Labeler proficient rx lp
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

progesterone 100 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-902
Product ID 71205-902_eb911dcf-c635-4133-9d70-db58b6636a97
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)
progesterone [epc]
Chemical Structure
progesterone [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205902
Hyphenated Format 71205-902

Supplemental Identifiers

RxCUI
260243 312641
UPC
0371205902308
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
  • 1000 CAPSULE in 1 BOTTLE (71205-902-11)
  • 30 CAPSULE in 1 BOTTLE (71205-902-30)
  • 500 CAPSULE in 1 BOTTLE (71205-902-55)
  • 60 CAPSULE in 1 BOTTLE (71205-902-60)
  • 120 CAPSULE in 1 BOTTLE (71205-902-72)
  • 90 CAPSULE in 1 BOTTLE (71205-902-90)
source: ndc

Packages (6)

Ingredients (1)

progesterone (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eb911dcf-c635-4133-9d70-db58b6636a97", "openfda": {"nui": ["M0017672", "N0000175601"], "upc": ["0371205902308"], "unii": ["4G7DS2Q64Y"], "rxcui": ["260243", "312641"], "spl_set_id": ["73e65b35-2266-48a3-98f8-521446a55c22"], "pharm_class_cs": ["Progesterone [CS]"], "pharm_class_epc": ["Progesterone [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (71205-902-11)", "package_ndc": "71205-902-11", "marketing_start_date": "20210720"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71205-902-30)", "package_ndc": "71205-902-30", "marketing_start_date": "20210720"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (71205-902-55)", "package_ndc": "71205-902-55", "marketing_start_date": "20210720"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71205-902-60)", "package_ndc": "71205-902-60", "marketing_start_date": "20210720"}, {"sample": false, "description": "120 CAPSULE in 1 BOTTLE (71205-902-72)", "package_ndc": "71205-902-72", "marketing_start_date": "20210720"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71205-902-90)", "package_ndc": "71205-902-90", "marketing_start_date": "20210720"}], "brand_name": "Progesterone", "product_id": "71205-902_eb911dcf-c635-4133-9d70-db58b6636a97", "dosage_form": "CAPSULE", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "71205-902", "generic_name": "Progesterone", "labeler_name": "Proficient Rx LP", "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": "20210108", "listing_expiration_date": "20261231"}