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12634-769 NDC - CIPROFLOXACIN ()

Drug Information

Product NDC: 12634-769

Proprietary Name: Ciprofloxacin

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Apotheca Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/9/2004

Package Information

No. Package Code Package Description Billing Unit
112634-769-0010 TABLET, FILM COATED in 1 BOTTLE (12634-769-00)
212634-769-01100 TABLET, FILM COATED in 1 BOTTLE (12634-769-01)
312634-769-5414 TABLET, FILM COATED in 1 BLISTER PACK (12634-769-54)
412634-769-5720 TABLET, FILM COATED in 1 BLISTER PACK (12634-769-57)
512634-769-5930 TABLET, FILM COATED in 1 BLISTER PACK (12634-769-59)
612634-769-6110 TABLET, FILM COATED in 1 BLISTER PACK (12634-769-61)
712634-769-666 TABLET, FILM COATED in 1 BLISTER PACK (12634-769-66)
812634-769-677 TABLET, FILM COATED in 1 BLISTER PACK (12634-769-67)
912634-769-7130 TABLET, FILM COATED in 1 BOTTLE (12634-769-71)
1012634-769-7424 TABLET, FILM COATED in 1 BOTTLE (12634-769-74)
1112634-769-7828 TABLET, FILM COATED in 1 BOTTLE (12634-769-78)
1212634-769-8020 TABLET, FILM COATED in 1 BOTTLE (12634-769-80)
1312634-769-8414 TABLET, FILM COATED in 1 BOTTLE (12634-769-84)
1412634-769-8515 TABLET, FILM COATED in 1 BOTTLE (12634-769-85)
1512634-769-911 TABLET, FILM COATED in 1 BLISTER PACK (12634-769-91)
1612634-769-966 TABLET, FILM COATED in 1 BOTTLE (12634-769-96)
1712634-769-988 TABLET, FILM COATED in 1 BOTTLE (12634-769-98)

NDC Record

Field Name Field Value Definition
PRODUCT NDC12634-769The 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.
PROPRIETARY NAMECiprofloxacinThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/9/2004This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEApotheca Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 5/3/2024
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