Ipratropium Bromide
- Product NDC
- 70518-1070
- 11-digit product format
- 705181070
- Labeler code
- 70518
- Product ID
- 70518-1070_c1320fb1-27c3-4d46-e053-2a95a90a6ed4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ipratropium Bromide
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075693
- Marketing category
- ANDA
- Marketing start
- 2019-03-19
- Marketing end
- 0000-00-00
- Substance
- IPRATROPIUM BROMIDE
- Active strength
- 1 mg/2.5mL
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1070-0 | 70518107000 | 2 POUCH in 1 CARTON (70518-1070-0) > 30 VIAL in 1 POUCH > 2.5 mL in 1 VIAL | 2 pouch | 2019-03-19 | 0000-00-00 | No | No | Current |