Albuterol
- Product NDC
- 51079-657
- 11-digit product format
- 510790657
- Labeler code
- 51079
- Product ID
- 51079-657_d0eb2d4c-02de-5a60-e053-2a95a90ac1cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA072894
- Marketing category
- ANDA
- Marketing start
- 1997-04-29
- Marketing end
- 2023-01-31
- Substance
- ALBUTEROL SULFATE
- Active strength
- 2 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 |
|---|
| 51079-657-20 | 51079065720 | 100 BLISTER PACK in 1 CARTON (51079-657-20) > 1 TABLET in 1 BLISTER PACK (51079-657-01) | 100 blister pack | 1997-04-29 | 0000-00-00 | No | No | Current |