FDA NDC Directory · JSON-LD · Markdown

ALLZITAL

NDC 68047-752 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namebutalbital and acetaminophen
Labeler / ManufacturerLarken Laboratories, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203484
Dosage form / routeTABLET · ORAL
Active ingredientsACETAMINOPHEN (325 mg/1)
BUTALBITAL (25 mg/1)
Marketing started20151204
Package count2

External sources

Source: openFDA. Public-domain (CC0).