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
- 71335-9739_3547019b-bb80-50a6-e063-6394a90ae40c
- Product NDC
- 71335-9739
- Form
- CAPSULE
- Composition / generic term
- PROGESTERONE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181128
- Source listing expiry
- 20261231
Source-listed ingredients
- PROGESTERONE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (71335-9739-1) · 71335-9739-1
- 8 CAPSULE in 1 BOTTLE (71335-9739-2) · 71335-9739-2
- 100 CAPSULE in 1 BOTTLE (71335-9739-3) · 71335-9739-3
- 10 CAPSULE in 1 BOTTLE (71335-9739-4) · 71335-9739-4
- 90 CAPSULE in 1 BOTTLE (71335-9739-5) · 71335-9739-5
- 60 CAPSULE in 1 BOTTLE (71335-9739-6) · 71335-9739-6
- 12 CAPSULE in 1 BOTTLE (71335-9739-7) · 71335-9739-7
- 180 CAPSULE in 1 BOTTLE (71335-9739-8) · 71335-9739-8
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.
Browse United States records →