24338-852 : Zenzedi 7.5 mg Oral Tablet
| NDC: | 24338-852 |
| Labeler: | Arbor Pharmaceuticals, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Zenzedi |
| Dosage Form: | Oral Tablet |
| Application #: | ANDA090533 |
| Rev. Date: | |
| CSA Schedule: | CII (US) [1] |
[1] Schedule II / IIN Controlled Substance: High potential for abuse which may lead to severe psychological or physical dependence. (i.e. Narcotics such as Dilaudid, Methadone, Demerol, Oxycodone, Percocet, Fentanyl, Morphine, Opium, Codeine, and Hydrocodone ... Schedule IIN stimulants include non-narcotic Amphetamines such as Dexedrine, Adderall, Desoxyn, Methylphenidate (Ritalin) ... Other Schedule II substances include Amobarbital, Glutethimide, and Pentobarbital. More Details: US Dept of Justice Controlled Substance Schedules.
Appearance:
| Markings: | 75;MIA |
| Shapes: |
Triangle (3 sides) |
| Colors: |
 Green |
| Size (mm): | 8 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
NDC Package Codes:
- 24338-852-03: 30 TABLET IN 1 BOTTLE (24338‑852‑03)
- 24338-852-10: 100 TABLET IN 1 BOTTLE (24338‑852‑10)
Active Ingredients:
- Dextroamphetamine Sulfate
Dosage Strength:
- 7.5 mg
Inactive Ingredients:
- Silicon Dioxide
- Crospovidone
- Cellulose, Microcrystalline
- Stearic Acid
- Fd&c Blue No. 1
- D&c Yellow No. 10
Pharmaceutical Classes:
- Central Nervous System Stimulant [EPC]
- Central Nervous System Stimulation [PE]
Related Products:
Based on records with the same trade name.- 24338-850 Zenzedi 2.5 mg Oral Tablet by Arbor Pharmaceuticals, Inc.
- 24338-851 Zenzedi 5 mg Oral Tablet by Arbor Pharmaceuticals, Inc.
- 24338-853 Zenzedi 10 mg Oral Tablet by Arbor Pharmaceuticals, Inc.
- 24338-854 Zenzedi 15 mg Oral Tablet by Arbor Pharmaceuticals, Inc.
- 24338-855 Zenzedi 20 mg Oral Tablet by Arbor Pharmaceuticals, Inc.
- 24338-856 Zenzedi 30 mg Oral Tablet by Arbor Pharmaceuticals, Inc.
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.