Cefadroxil

Product NDC: 63629-7615
11-digit product format: 636297615
Labeler code: 63629
Product ID: 63629-7615_e46ef026-5773-4599-93e4-b6c5ad26341c
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Cefadroxil
Dosage form: CAPSULE
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA065352
Marketing category: ANDA
Marketing start: 2007-01-25
Marketing end: 0000-00-00
Substance: CEFADROXIL
Active strength: 500 mg/1
Pharmacologic classes: Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63629-7615-1	2020-10-16	C162847	48780-1	9d75b9d0-3811-f424-e053-dadaa90a57ce	2caab458-4e9e-481b-8196-09d23425e205
63629-7615-1	2020-01-31	C162847	48780-1	9d75b9d0-3811-f424-e053-dadaa90a57ce	2caab458-4e9e-481b-8196-09d23425e205

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
280111G160	CEFADROXIL	66592-87-8	CEFADROXIL

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63629-7615-1	63629761501	20 CAPSULE in 1 BOTTLE (63629-7615-1)	20 capsule	2018-05-25	0000-00-00	No	No	Current