0527-1552 NDC - BUTALBITAL, ASPIRIN, AND CAFFEINE

Drug Information

Product NDC: 0527-1552

Proprietary Name: Butalbital, aspirin, and caffeine

Non Proprietary Name: Butalbital, aspirin, and caffeine

Active Ingredient(s):
  • 50 mg/1 BUTALBITAL;
  • 325 mg/1 ASPIRIN;
  • 40 mg/1 CAFFEINE


Administration Route(s): ORAL

Dosage Form(s): CAPSULE

Pharmacy Class(es):
  • Barbiturate [EPC];
  • Barbiturates [Chemical/Ingredient];
  • Cyclooxygenase Inhibitors [MoA];
  • Decreased Prostaglandin Production [PE];
  • Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient];
  • Nonsteroidal Anti-inflammatory Drug [EPC];
  • Platelet Aggregation Inhibitor [EPC];
  • Decreased Platelet Aggregation [PE];
  • Central Nervous System Stimulant [EPC];
  • Central Nervous System Stimulation [PE];
  • Methylxanthine [EPC];
  • Xanthines [Chemical/Ingredient]

Labeler Information

Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086996
Marketing Category: ANDA
Start Marketing Date:10/11/1985
DEA Schedule:CIII

Package Information

No. Package Code Package Description Billing Unit
10527-1552-01100 CAPSULE in 1 BOTTLE (0527-1552-01)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC0527-1552The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEButalbital, aspirin, and caffeineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEButalbital, aspirin, and caffeineThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECAPSULEThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE10/11/1985This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERANDA086996This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMELannett Company, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEBUTALBITAL; ASPIRIN; CAFFEINEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH50; 325; 40 
ACTIVE INGRED UNITmg/1; mg/1; mg/1 
PHARM CLASSESBarbiturate [EPC],Barbiturates [Chemical/Ingredient],Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC],Platelet Aggregation Inhibitor [EPC],Decreased Platelet Aggregation [PE],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient] 
DEA SCHEDULECIIIThis is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.

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This page was last updated on: 10/2/2018