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NDC 50090-5968-00 Ipratropium Bromide 42 ug/1 Details
Ipratropium Bromide 42 ug/1
Ipratropium Bromide is a NASAL SPRAY, METERED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is IPRATROPIUM BROMIDE.
MedlinePlus Drug Summary
Ipratropium nasal spray is available in two strengths that are used to treat different conditions. Ipratropium nasal spray 0.06% is used to relieve a runny nose caused by the common cold or seasonal allergies (hay fever) in adults and children age 5 and older. Ipratropium nasal spray 0.03% is used to relieve a runny nose caused by year-round allergic and nonallergic rhinitis (runny nose and stuffiness) in adults and children age 6 and older. Ipratropium nasal spray does not relieve nasal congestion, sneezing, or postnasal drip caused by these conditions. Ipratropium nasal spray is in a class of medications called anticholinergics. It works by reducing the amount of mucus produced in the nose.
Related Packages: 50090-5968-00Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Ipratropium Nasal Spray
Product Information
| NDC | 50090-5968 |
|---|---|
| Product ID | 50090-5968_08f74948-1549-4dd3-b93f-be28dbd3e097 |
| Associated GPIs | |
| GCN Sequence Number | 024456 |
| GCN Sequence Number Description | ipratropium bromide SPRAY 42 MCG NASAL |
| HIC3 | Q7A |
| HIC3 Description | NOSE PREPARATIONS, MISCELLANEOUS (RX) |
| GCN | 42238 |
| HICL Sequence Number | 000057 |
| HICL Sequence Number Description | IPRATROPIUM BROMIDE |
| Brand/Generic | Generic |
| Proprietary Name | Ipratropium Bromide |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | ipratropium bromide |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | SPRAY, METERED |
| Route | NASAL |
| Active Ingredient Strength | 42 |
| Active Ingredient Units | ug/1 |
| Substance Name | IPRATROPIUM BROMIDE |
| Labeler Name | A-S Medication Solutions |
| Pharmaceutical Class | Anticholinergic [EPC], Cholinergic Antagonists [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA076155 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50090-5968-00 (50090596800)
| NDC Package Code | 50090-5968-0 |
|---|---|
| Billing NDC | 50090596800 |
| Package | 1 BOTTLE, PUMP in 1 CARTON (50090-5968-0) / 165 SPRAY, METERED in 1 BOTTLE, PUMP |
| Marketing Start Date | 2022-04-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |