12634-184 NDC - PREDNISONE ()

Drug Information

Product NDC: 12634-184

Proprietary Name: Prednisone

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:5/22/1972

Package Information

No. Package Code Package Description Billing Unit
112634-184-0010 TABLET in 1 BOTTLE (12634-184-00)
212634-184-01100 TABLET in 1 BOTTLE (12634-184-01)
312634-184-0935 TABLET in 1 BOTTLE (12634-184-09)
412634-184-4040 TABLET in 1 BOTTLE (12634-184-40)
512634-184-4242 TABLET in 1 BOTTLE (12634-184-42)
612634-184-5050 TABLET in 1 BOTTLE (12634-184-50)
712634-184-5212 TABLET in 1 BLISTER PACK (12634-184-52)
812634-184-5414 TABLET in 1 BOTTLE (12634-184-54)
912634-184-5720 TABLET in 1 BLISTER PACK (12634-184-57)
1012634-184-5930 TABLET in 1 BOTTLE (12634-184-59)
1112634-184-6060 TABLET in 1 BOTTLE (12634-184-60)
1212634-184-6110 TABLET in 1 BLISTER PACK (12634-184-61)
1312634-184-633 TABLET in 1 BLISTER PACK (12634-184-63)
1412634-184-666 TABLET in 1 BLISTER PACK (12634-184-66)
1512634-184-677 TABLET in 1 BLISTER PACK (12634-184-67)
1612634-184-699 TABLET in 1 BLISTER PACK (12634-184-69)
1712634-184-7130 TABLET in 1 BOTTLE (12634-184-71)
1812634-184-7424 TABLET in 1 BOTTLE (12634-184-74)
1912634-184-7828 TABLET in 1 BOTTLE (12634-184-78)
2012634-184-7925 TABLET in 1 BOTTLE (12634-184-79)
2112634-184-8020 TABLET in 1 BOTTLE (12634-184-80)
2212634-184-8121 TABLET in 1 BOTTLE (12634-184-81)
2312634-184-8212 TABLET in 1 BOTTLE (12634-184-82)
2412634-184-8515 TABLET in 1 BOTTLE (12634-184-85)
2512634-184-911 TABLET in 1 BLISTER PACK (12634-184-91)
2612634-184-944 TABLET in 1 BOTTLE (12634-184-94)
2712634-184-955 TABLET in 1 BOTTLE (12634-184-95)
2812634-184-966 TABLET in 1 BOTTLE (12634-184-96)

NDC Record

Field Name Field Value Definition
PRODUCT NDC12634-184The 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 NAMEPrednisoneThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/22/1972This 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: 2/1/2023