ReadySharp Betamethasone

Product NDC

68788-7327

11-digit product format

687887327

Labeler code

68788

Product ID

68788-7327_5f929a49-6577-490e-87eb-258d5e4a8e94

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Betamethasone Sodium Phosphate and Betamethasone Acetate

Dosage form

INJECTION, SUSPENSION

Route

INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA090747

Marketing category

ANDA

Marketing start

2019-03-12

Marketing end

0000-00-00

Substance

BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE

Active strength

3 mg/mL; mg/mL

Pharmacologic classes

Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record