70538-450 : Allzital Oral Tablet

Labeler: Keswick Labs, LLC
Product Type: Human Prescription Drug
Drug Name:  Allzital
Dosage Form: Oral Tablet
Application #: ANDA203484
Rev. Date: 


Markings: LL722
Shapes:  Oval
Colors:  White
Size (mm): 16
Segments: * 0

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 0 indicates a scored pill which can be broken into 0 equal pieces.

NDC Package Codes:

  • 70538-450-01: 100 MG IN 1 BOTTLE (70538‑450‑01)

Active Ingredients:

  • Butalbital
  • Acetaminophen

Dosage Strength:

  • 25 mg/mg
  • 325 mg/mg

Inactive Ingredients:

  • Povidone
  • Croscarmellose Sodium
  • Crospovidone
  • Cellulose, Microcrystalline
  • Starch, Pregelatinized Corn
  • Stearic Acid
  • Silicon Dioxide
  • Magnesium Stearate

Pharmaceutical Classes:

  • Barbiturate [EPC]
  • Barbiturates [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
  • 68047-722 Allzital Oral Tablet by Larken Laboratories, Inc.
  • 68047-752 Allzital Oral Tablet by Larken Laboratories, Inc.
  • 70362-722 Allzital Oral Tablet by Skylar Laboratories, LLC
  • 70569-150 Allzital Oral Tablet by Phlight Pharma, LLC


Scan the QR code below to easily reference this data in the future:

NDC 70538-450 QR Code

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Note: The MedsChat® 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.