Cromolyn Sodium

Product NDC

63187-473

11-digit product format

631870473

Labeler code

63187

Product ID

63187-473_e16e8e4b-e959-4315-8633-5c1c536cde39

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

cromolyn sodium

Dosage form

SOLUTION/ DROPS

Route

OPHTHALMIC

Labeler

Proficient Rx LP

Application

ANDA074443

Marketing category

ANDA

Marketing start

1998-05-26

Marketing end

0000-00-00

Substance

CROMOLYN SODIUM

Active strength

40 mg/mL

Pharmacologic classes

Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record