Cromolyn Sodium

Product NDC

0904-5532

11-digit product format

009045532

Labeler code

0904

Product ID

0904-5532_9857e24e-871d-445d-8b52-c18643aa32bd

Type

HUMAN OTC DRUG

Nonproprietary name

Cromolyn Sodium

Dosage form

SPRAY, METERED

Route

NASAL

Labeler

Major Pharmaceuticals

Application

ANDA075702

Marketing category

ANDA

Marketing start

2001-07-03

Marketing end

0000-00-00

Substance

CROMOLYN SODIUM

Active strength

5 mg/mL

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record