Cephalexin

Product NDC
68788-7271
11-digit product format
687887271
Labeler code
68788
Product ID
68788-7271_45fad574-3623-49d2-b88d-cd325ad1a084
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cephalexin
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA065152
Marketing category
ANDA
Marketing start
2019-01-10
Marketing end
0000-00-00
Substance
CEPHALEXIN
Active strength
250 mg/5mL
Pharmacologic classes
Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7271-1ML - Milliliter68788-7271e5bb9ac2-ce3f-49d0-94b5-7f18a7e17f6612019-04-11
68788-7271-2ML - Milliliter68788-727102c22311-b161-4100-839c-be6e5070028b12019-04-11