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Ipratroprium Bromide

NDC 68682-398 · Oceanside Pharmaceuticals

Generic nameIpratroprium Bromide
Dosage formSPRAY, METERED
RouteNASAL
Active ingredient(s)IPRATROPIUM BROMIDE
Strength21 ug/1
Pharmacologic classAnticholinergic [EPC], Cholinergic Antagonists [MoA]
Marketing categoryANDA

Packages

68682-398-30 — 1 BOTTLE, SPRAY in 1 CARTON (68682-398-30) / 345 SPRAY, METERED in 1 BOTTLE, SPRAY

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60687-405 — Ipratropium Bromide and Albuterol Sulfate, 62135-830 — Ipratropium Bromide, 62135-831 — Ipratropium Bromide and Albuterol Sulfate, 64980-640 — Ipratropium Bromide, 64980-645 — Ipratropium Bromide and Albuterol Sulfate, 65862-905 — Ipratropium bromide, 65862-906 — Ipratropium Bromide and Albuterol Sulfate, 67296-2246 — Ipratropium Bromide, 67296-2315 — Ipratropium Bromide and Albuterol Sulfate, 68071-3769 — Ipratropium Bromide, 68682-399 — Ipratropium Bromide, 68788-8103 — Ipratropium Bromide and Albuterol Sulfate, 69097-173 — Ipratropium Bromide and Albuterol Sulfate, 69097-840 — Ipratropium Bromide and Albuterol Sulfate, 69238-2016 — Ipratropium Bromide, 69238-2017 — Ipratropium Bromide, 70748-336 — IPRATROPIUM BROMIDE, 70748-337 — IPRATROPIUM BROMIDE, 71205-051 — Ipratropium Bromide and Albuterol Sulfate, 71205-726 — Ipratropium Bromide and Albuterol Sulfate, +33 more

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