PROAIR
- Product NDC
- 70518-1230
- 11-digit product format
- 705181230
- Labeler code
- 70518
- Product ID
- 70518-1230_c197c0f6-c748-5732-e053-2a95a90a2550
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- REMEDYREPACK INC.
- Application
- NDA021457
- Marketing category
- NDA
- Marketing start
- 2018-05-29
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 90 ug/1
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1230 | PROAIR HFA (ALBUTEROL SULFATE) AEROSOL, METERED [REMEDYREPACK INC.] | 5 | Legacy NDC | 20210506_949f9663-f4e7-499f-9329-49462ff55c0e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1230-0 | 70518123000 | 1 INHALER in 1 CARTON (70518-1230-0) > 200 AEROSOL, METERED in 1 INHALER | 1 inhaler | 2018-05-29 | 0000-00-00 | No | No | Current |