ALBUTEROL SULFATE
- Product NDC
- 51662-1202
- 11-digit product format
- 516621202
- Labeler code
- 51662
- Product ID
- 51662-1202_9ef31030-4d32-3f8c-e053-2995a90aea61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALBUTEROL SULFATE
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Application
- NDA021457
- Marketing category
- NDA
- Marketing start
- 2018-10-18
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51662-1202-1 | 51662120201 | 200 AEROSOL, METERED in 1 INHALER (51662-1202-1) | | 2018-10-18 | 0000-00-00 | No | No | Current |
| 51662-1202-9 | 51662120209 | 1 INHALER in 1 CARTON (51662-1202-9) > 200 AEROSOL, METERED in 1 INHALER | 1 inhaler | 2019-01-19 | 0000-00-00 | No | No | Current |