Cephalexin

Product NDC: 72162-2145
11-digit product format: 721622145
Labeler code: 72162
Product ID: 72162-2145_58759ee9-29d7-4b3e-8b95-d4857eeffadd
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Cephalexin
Dosage form: CAPSULE
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA062702
Marketing category: ANDA
Marketing start: 1990-09-30
Substance: CEPHALEXIN
Active strength: 500 mg/1
Pharmacologic classes: Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

openFDA Listing Details

Product ID: 72162-2145_58759ee9-29d7-4b3e-8b95-d4857eeffadd
SPL ID: 58759ee9-29d7-4b3e-8b95-d4857eeffadd
Product type: HUMAN PRESCRIPTION DRUG
Finished product: Yes
Brand name base: Cephalexin
Generic name: Cephalexin
Dosage form: CAPSULE
Route: ORAL
Marketing start: 1990-09-30
Marketing category: ANDA
Application number: ANDA062702
Pharmacologic classes: Cephalosporin Antibacterial [EPC]; Cephalosporins [CS]
Listing expiration: 2026-12-31

Ingredient	Strength
CEPHALEXIN	500 mg/1

Package NDC	Description	Marketing start	Sample
72162-2145-5	500 CAPSULE in 1 BOTTLE (72162-2145-5)	2023-12-07	No

UNII	Preferred term	Registry number	Matched term
OBN7UDS42Y	CEPHALEXIN	23325-78-2	CEPHALEXIN

Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
72162-2145-5	72162214505	500 CAPSULE in 1 BOTTLE (72162-2145-5)	500 capsule	2023-12-07	No	No	Historical

Title	Manufacturer	Effective date	Type	Version
Cephalexin	Bryant Ranch Prepack	2023-12-07	HUMAN PRESCRIPTION DRUG LABEL	100