VENTOLIN
- Product NDC
- 70518-1081
- 11-digit product format
- 705181081
- Labeler code
- 70518
- Product ID
- 70518-1081_485918a3-f680-2d1c-e063-6294a90a00e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- albuterol sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- REMEDYREPACK INC.
- Application
- NDA020983
- Marketing category
- NDA
- Marketing start
- 2018-03-24
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- VENTOLIN
- Brand name suffix
- HFA
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALBUTEROL SULFATE | 90 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 021SEF3731 |
| Rxcui | 859088, 2123076 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-1081-0 | VENTOLINHFA | 200 in 1 INHALER | AEROSOL, METERED | 200 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1081 | VENTOLIN HFA (ALBUTEROL SULFATE) AEROSOL, METERED [REMEDYREPACK INC.] | 12 | Current NDC, Legacy NDC, 1 package rows | 20250507_adb8d669-b91c-46f1-8a86-19f504840eff.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1081-0 | 70518108100 | 200 AEROSOL, METERED in 1 INHALER (70518-1081-0) | 2018-03-24 | 0000-00-00 | No | No | Current |