United States · FDA National Drug Code directory

PROGESTERONE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
72189-347_2c4c6aca-4b89-7f9f-e063-6394a90a0a23
Product NDC
72189-347
Form
CAPSULE
Composition / generic term
PROGESTERONE
Labeler
Direct Rx
Marketing category
ANDA
Marketing start / end (source format)
20220414
Source listing expiry
20261231

Source-listed ingredients

  • PROGESTERONE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

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

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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PROGESTERONE — United States | Molindra Medicines