Cefdinir

Product NDC: 68001-150
11-digit product format: 680010150
Labeler code: 68001
Product ID: 68001-150_b0d198ac-6b9b-4bc4-99e8-5640be67289a
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Cefdinir
Dosage form: CAPSULE
Route: ORAL
Labeler: BluePoint Laboratories
Application: ANDA065264
Marketing category: ANDA
Marketing start: 2014-02-07
Marketing end: 0000-00-00
Substance: CEFDINIR
Active strength: 300 mg/1
Pharmacologic classes: Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d3e72f63-2c41-955f-f4ce-e90c6403e67c	Product name	2	20210729
e8e66e64-d220-99cb-44eb-0f32dc8cbda1	Product name	2	20210729

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
68001-150-06	EA - Each	68001-150	5be32d9c-c300-44c0-9571-edeb8312968c	1	2014-04-03

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
CI0FAO63WC	CEFDINIR	91832-40-5	CEFDINIR

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
200346	cefdinir 300 MG Oral Capsule	PSN	71da826c-5a04-4ba0-a5c7-dd294f9b0532	3
200346	cefdinir 300 MG Oral Capsule	SCD	71da826c-5a04-4ba0-a5c7-dd294f9b0532	3

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
68001-150-06	68001015006	60 CAPSULE in 1 BOTTLE (68001-150-06)	60 capsule	2014-02-07	0000-00-00	No	No	Current