Orange Book product
AMPHETAMINE SULFATE 10MG
Orange Book ANDA 213583 · SPECGX LLC · Prescription
Key facts
| Proprietary name | AMPHETAMINE SULFATE |
|---|---|
| Active ingredients | AMPHETAMINE SULFATE |
| Strength | 10MG |
| Dosage form | TABLET |
| Route | ORAL |
| Application | ANDA213583 |
| Applicant holder | SPECGX LLC |
| Marketing status | Prescription |
| Therapeutic equivalence (TE) code | AA |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Jan 22, 2021 |
At a glance
- 10–99 Marketed products with the same ingredient, strength and form
- 1–9 Products in this application
- No Reference listed drug
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Orange Book products
The FDA Orange Book lists approved drug products with their therapeutic equivalence (TE) codes, reference listed drugs and marketing status. Products approved before 1982 show an approval date of Jan 1, 1982.