Prescription drug · ANDA
albuterol sulfate NDC 51407-367
Albuterol sulfate 2 mg/1 · Tablet · Oral · Golden State Medical Supply, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 51407-367-01 | 51407036701 | 100 TABLET in 1 BOTTLE (51407-367-01)Marketed from Mar 26, 2020 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- albuterol sulfate
- Generic name (nonproprietary)
- albuterol sulfate
- Active ingredients
- Albuterol sulfate — 2 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 072637
- Marketing start
- Listing expires
- Other FDA classes
- Adrenergic beta2-Agonists (Mechanism)
- Identifiers
- Product ID 51407-367_4f875ac2-2a69-dbc3-e063-6394a90a31f1SPL ID 4f875ac2-2a69-dbc3-e063-6394a90a31f1SPL set ID a22af54a-c010-ab8b-e053-2a95a90a8862RxCUI 197316, 197318UNII 021SEF3731
- Pharmacologic class
- beta2-Adrenergic Agonist
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N451407036701followed by a unit qualifier and the quantityPackage 51407-0367-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS AND USAGE Albuterol tablets are indicated for the relief of bronchospasm in adults and children 6 years of age and older with reversible obstructive airway disease.
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 072637
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| albuterol sulfate | Albuterol sulfate 2 mg/1 | TabletOral | Sun Pharmaceutical Industries, Inc. | 53489-176 |
| albuterol sulfate | Albuterol sulfate 4 mg/1 | TabletOral | Sun Pharmaceutical Industries, Inc. | 53489-177 |
| albuterol sulfate | Albuterol sulfate 4 mg/1 | TabletOral | Golden State Medical Supply, Inc. | 51407-368 |
| Albuterol Sulfate | Albuterol sulfate 2 mg/1 | TabletOral | American Health Packaging | 68084-949 |