68047-752 : Allzital Oral Tablet


NDC68047-752
Labeler: Larken Laboratories, Inc.
Product Type: Human Prescription Drug
Drug Name:  Allzital
Dosage Form: Oral Tablet
Application #: ANDA203484
Rev. Date: 
CSA Schedule: CIII (US) [1]


[1] Schedule III / IIIN Controlled Substance: Has a potential for abuse less than substances in Schedules I or II and abuse may lead to moderate or low physical dependence or high psychological dependence. (i.e. Products containing not more than 90 milligrams of Codeine per dosage unit [such as Tylenol with Codeine], other narcotics such as Buprenorphine (Suboxone), and Schedule IIIN non-narcotics such as Didrex, Ketamine, Phendimetrazine, and Anabolic Steroids). More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

  • 68047-752-01: 100 TABLET IN 1 BOTTLE (68047‑752‑01)
  • 68047-752-30: 30 TABLET IN 1 BOTTLE (68047‑752‑30)

Active Ingredients:

  • Butalbital
  • Acetaminophen

Dosage Strength:

  • 25 mg
  • 325 mg

Pharmaceutical Classes:

  • Barbiturates [CS]
  • Barbiturate [EPC]

Related Products:

Based on records with the same trade name.
  • 68047-722 Allzital Oral Tablet by Larken Laboratories, Inc.
  • 70362-722 Allzital Oral Tablet by Skylar Laboratories, LLC
  • 70538-450 Allzital Oral Tablet by Keswick Labs, LLC
  • 70569-150 Allzital Oral Tablet by Phlight Pharma, LLC

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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.