progesterone

Generic: progesterone

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name progesterone
Generic Name progesterone
Labeler nucare pharmaceuticals,inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

progesterone 200 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3529
Product ID 68071-3529_42b5544c-f065-7758-e063-6394a90a20ef
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200900
Listing Expiration 2026-12-31
Marketing Start 2018-11-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713529
Hyphenated Format 68071-3529

Supplemental Identifiers

RxCUI
312641
UPC
0368071352993
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 ANDA200900 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (68071-3529-3)
  • 60 CAPSULE in 1 BOTTLE (68071-3529-6)
  • 180 CAPSULE in 1 BOTTLE (68071-3529-8)
  • 90 CAPSULE in 1 BOTTLE (68071-3529-9)
source: ndc

Packages (4)

Ingredients (1)

progesterone (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42b5544c-f065-7758-e063-6394a90a20ef", "openfda": {"nui": ["M0017672", "N0000175601"], "upc": ["0368071352993"], "unii": ["4G7DS2Q64Y"], "rxcui": ["312641"], "spl_set_id": ["0b3da881-4720-cdee-e063-6394a90aee99"], "pharm_class_cs": ["Progesterone [CS]"], "pharm_class_epc": ["Progesterone [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68071-3529-3)", "package_ndc": "68071-3529-3", "marketing_start_date": "20231128"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (68071-3529-6)", "package_ndc": "68071-3529-6", "marketing_start_date": "20251103"}, {"sample": false, "description": "180 CAPSULE in 1 BOTTLE (68071-3529-8)", "package_ndc": "68071-3529-8", "marketing_start_date": "20251009"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (68071-3529-9)", "package_ndc": "68071-3529-9", "marketing_start_date": "20231128"}], "brand_name": "PROGESTERONE", "product_id": "68071-3529_42b5544c-f065-7758-e063-6394a90a20ef", "dosage_form": "CAPSULE", "pharm_class": ["Progesterone [CS]", "Progesterone [EPC]"], "product_ndc": "68071-3529", "generic_name": "PROGESTERONE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROGESTERONE", "active_ingredients": [{"name": "PROGESTERONE", "strength": "200 mg/1"}], "application_number": "ANDA200900", "marketing_category": "ANDA", "marketing_start_date": "20181128", "listing_expiration_date": "20261231"}