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Miconazole 7

NDC 61269-730 · H2-Pharma, LLC

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameMiconazole Nitrate
Dosage formCREAM
RouteVAGINAL
Active ingredient(s)MICONAZOLE NITRATE
Strength20 mg/g
Pharmacologic classAzole Antifungal [EPC], Azoles [CS]
Marketing categoryANDA

Packages

61269-730-41 — 1 TUBE, WITH APPLICATOR in 1 CARTON (61269-730-41) / 45 g in 1 TUBE, WITH APPLICATOR

61269-730-63 — 1 TUBE, WITH APPLICATOR in 1 CARTON (61269-730-63) / 45 g in 1 TUBE, WITH APPLICATOR

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59088-238 — MICONAZOLE NITRATE 2% Antifungal, 59088-239 — MICONAZOLE NITRATE 2% Antifungal, 59088-442 — Miconazole Nitrate, 59088-478 — Miconazole Nitrate, 59208-001 — Miconazole Nitrate, 59640-101 — Miconazole Nitrate, 59726-988 — Miconazole Nitrate, 59779-097 — Athletes Foot Spray, 60232-0009 — 2% Miconazole Nitrate Cream, 60232-0046 — miconazole nitrate antifungal cream, 62654-147 — MICONAZOLE NITRATE, 63347-380 — MICONAZOLE NITRATE, 63347-470 — MICONAZOLE NITRATE, 63347-810 — MICONAZOLE NITRATE, 63736-015 — Miconazole Nitrate, 63736-025 — Miconazole Nitrate, 63736-026 — Miconazole Nitrate, 63742-098 — MICONAZOLE NITRATE, 63868-180 — Athletes Foot Powder Spray Talc Free, 63868-198 — Miconazole Nitrate, +223 more

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