Betamethasone Sodium Phosphate and Betamethasone Acetate

Product NDC

70518-0506

11-digit product format

705180506

Labeler code

70518

Product ID

70518-0506_a4e26729-d5b3-0d9c-e053-2a95a90aafe6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Betamethasone Sodium Phosphate and Betamethasone Acetate

Dosage form

INJECTION, SUSPENSION

Route

INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR

Labeler

REMEDYREPACK INC.

Application

ANDA090747

Marketing category

ANDA

Marketing start

2017-05-09

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

2021-12-31

Current FDA listing

Historical FDA.report record