Cephalexin

Product NDC: 71335-2877
11-digit product format: 713352877
Labeler code: 71335
Product ID: 71335-2877_67075da3-3dd1-4794-833c-af7e1058c9d4
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Cephalexin
Dosage form: FOR SUSPENSION
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA210221
Marketing category: ANDA
Marketing start: 2019-03-28
Substance: CEPHALEXIN
Active strength: 250 mg/5mL
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: 71335-2877_67075da3-3dd1-4794-833c-af7e1058c9d4
SPL ID: 67075da3-3dd1-4794-833c-af7e1058c9d4
Product type: HUMAN PRESCRIPTION DRUG
Finished product: Yes
Brand name base: Cephalexin
Generic name: Cephalexin
Dosage form: FOR SUSPENSION
Route: ORAL
Marketing start: 2019-03-28
Marketing category: ANDA
Application number: ANDA210221
Pharmacologic classes: Cephalosporin Antibacterial [EPC]; Cephalosporins [CS]
Listing expiration: 2026-12-31

Ingredient	Strength
CEPHALEXIN	250 mg/5mL

Package NDC	Description	Marketing start	Sample
71335-2877-1	200 mL in 1 BOTTLE (71335-2877-1)	2025-11-07	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
71335-2877-1	71335287701	200 mL in 1 BOTTLE (71335-2877-1)	200 ml	2025-11-07	No	No	Historical

Title	Manufacturer	Effective date	Type	Version
Cephalexin	Bryant Ranch Prepack	2025-11-07	HUMAN PRESCRIPTION DRUG LABEL	100