54868-3313 NDC - PERIOGARD ()

Drug Information

  • Product NDC: 54868-3313
  • Proprietary Name: Periogard
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Physicians Total Care, Inc.
Product Type:
FDA Application Number: ANDA073695
Marketing Category: ANDA
Start Marketing Date:1/25/1995
End Marketing Date:6/30/2011

Package Information

No. Package Code Package Description Billing Unit
154868-3313-0473 mL in 1 BOTTLE (54868-3313-0)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC54868-3313The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAMEPeriogardThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/25/1995This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE6/30/2011The translation of the route code submitted by the firm, indicating route of administration.
MARKETING CATEGORY NAMEANDAThis is the date that the labeler indicates was the start of its marketing of the drug product.
APPLICATION NUMBERANDA073695This 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 NAMEPhysicians Total Care, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/21/2025