Albuterol Sulfate
- Product NDC
- 0781-7155
- 11-digit product format
- 007817155
- Labeler code
- 0781
- Product ID
- 0781-7155_5fb1a243-8c4d-d584-e053-2991aa0ae1cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Sandoz Inc.
- Application
- ANDA077839
- Marketing category
- ANDA
- Marketing start
- 2011-08-17
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 3 mg/3mL
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0781-7155-29 | 2022-03-02 | C162847 | 48780-1 | 9d75b9d0-f30d-f424-e053-dadaa90a57ce | cad98bce-bb10-4a04-94e7-d6f55ae60cda |
| 0781-7155-64 | 2022-03-02 | C162847 | 48780-1 | 9d75b9d0-f30d-f424-e053-dadaa90a57ce | cad98bce-bb10-4a04-94e7-d6f55ae60cda |
| 0781-7155-86 | 2022-03-02 | C162847 | 48780-1 | 9d75b9d0-f30d-f424-e053-dadaa90a57ce | cad98bce-bb10-4a04-94e7-d6f55ae60cda |
| 0781-7155-29 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-f30d-f424-e053-dadaa90a57ce | cad98bce-bb10-4a04-94e7-d6f55ae60cda |
| 0781-7155-64 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-f30d-f424-e053-dadaa90a57ce | cad98bce-bb10-4a04-94e7-d6f55ae60cda |
| 0781-7155-86 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-f30d-f424-e053-dadaa90a57ce | cad98bce-bb10-4a04-94e7-d6f55ae60cda |