50090-1913 : Diazepam 5 mg Oral Tablet


NDC50090-1913
Labeler: A-s Medication Solutions
Product Type: Human Prescription Drug
Drug Name:  Diazepam
Dosage Form: Oral Tablet
Application #: ANDA071321
Rev. Date: 
CSA Schedule: CIV (US) [1]


[1] Schedule IV Controlled Substance: Low potential for abuse relative to substances in Schedule III. Examples include Alprazolam (Xanax), Diazepam (Valium), Carisoprodol (Soma), Clonazepam (Klonopin), Lorazepam (Ativan), Clorazepate (Tranxene), Midazolam (Versed), Temazepam (Restoril), and Triazolam (Halcion).. More Details: US Dept of Justice Controlled Substance Schedules.

Appearance:


Markings: 3926;TEVA
Shapes:  Round
Colors:  Yellow
Size (mm): 8
Segments: * 2

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

3926 TEVA: (0172-3926) Diazepam 5 mg Oral Tablet by A-s Medication Solutions
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 50090-1913-0: 15 TABLET IN 1 BOTTLE (50090‑1913‑0)
  • 50090-1913-1: 20 TABLET IN 1 BOTTLE (50090‑1913‑1)
  • 50090-1913-2: 30 TABLET IN 1 BOTTLE (50090‑1913‑2)
  • 50090-1913-3: 60 TABLET IN 1 BOTTLE (50090‑1913‑3)
  • 50090-1913-4: 10 TABLET IN 1 BOTTLE (50090‑1913‑4)
  • 50090-1913-5: 100 TABLET IN 1 BOTTLE (50090‑1913‑5)
  • 50090-1913-6: 50 TABLET IN 1 BOTTLE (50090‑1913‑6)
  • 50090-1913-7: 6 TABLET IN 1 BOTTLE (50090‑1913‑7)
  • 50090-1913-8: 3 TABLET IN 1 BOTTLE (50090‑1913‑8)
  • 50090-1913-9: 12 TABLET IN 1 BOTTLE (50090‑1913‑9)

Active Ingredients:

  • Diazepam

Dosage Strength:

  • 5 mg

Inactive Ingredients:

  • Anhydrous Lactose
  • Silicon Dioxide
  • D&c Yellow No. 10
  • Aluminum Oxide
  • Fd&c Yellow No. 6
  • Magnesium Stearate
  • Microcrystalline Cellulose
  • Starch, Corn
  • Sodium Starch Glycolate Type a Potato

Pharmaceutical Classes:

  • Benzodiazepine [EPC]
  • Benzodiazepines [CS]

Related Products:

Based on records with the same trade name.
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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.