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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