Albuterol
- Product NDC
- 55289-045
- 11-digit product format
- 552890045
- Labeler code
- 55289
- Product ID
- 55289-045_dcf4fe82-c5f5-8cf1-e053-2995a90a0ec2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- albuterol sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA072894
- Marketing category
- ANDA
- Marketing start
- 1991-01-17
- Marketing end
- 2023-02-28
- Substance
- ALBUTEROL SULFATE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 55289-045-30 | 55289004530 | 30 TABLET in 1 BOTTLE, PLASTIC (55289-045-30) | 30 tablet | 2011-05-04 | 0000-00-00 | No | No | Current |