albuterol sulfate
- Product NDC
- 68788-0255
- 11-digit product format
- 687880255
- Labeler code
- 68788
- Product ID
- 68788-0255_a74b07d9-0fbd-4f1a-806a-9f253cbd5ba3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- albuterol sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA072637
- Marketing category
- ANDA
- Marketing start
- 1989-12-05
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record