Skip to main content

Progesterone

NDC 71205-902 · Proficient Rx LP

Generic nameProgesterone
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PROGESTERONE
Strength100 mg/1
Pharmacologic classProgesterone [CS], Progesterone [EPC]
Marketing categoryANDA

Packages

71205-902-11 — 1000 CAPSULE in 1 BOTTLE (71205-902-11)

71205-902-30 — 30 CAPSULE in 1 BOTTLE (71205-902-30)

71205-902-55 — 500 CAPSULE in 1 BOTTLE (71205-902-55)

71205-902-60 — 60 CAPSULE in 1 BOTTLE (71205-902-60)

71205-902-72 — 120 CAPSULE in 1 BOTTLE (71205-902-72)

71205-902-90 — 90 CAPSULE in 1 BOTTLE (71205-902-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-2560 — Progesterone, 70518-4166 — PROGESTERONE, 70518-4552 — Progesterone, 70558-0008 — Acetaldehyde, Dopamine Hydrochloride, DHEA (Dehydroepiandrosterone), 7-Oxo- Dehydroepiandrosterone 3-Acetate, Folliculinum, Oophorinum (Suis), Cholesterinum, Progesterone, Testosterone, Cortisone Aceticum, Aldosterone, Androsterone, Follicle Stimulating Hormone, 70700-162 — Progesterone, 70700-163 — Progesterone, 70700-201 — Progesterone, 70700-286 — PROGESTERONE, 71205-669 — Progesterone, 71205-684 — Progesterone, 71205-903 — Progesterone, 71335-1406 — Progesterone, 71335-1432 — Progesterone, 71335-1443 — Progesterone, 71335-1913 — Progesterone, 71335-1990 — Progesterone, 71335-2242 — PROGESTERONE, 71335-9739 — PROGESTERONE, 72189-204 — PROGESTERONE, 72189-217 — PROGESTERONE, +106 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.