Brucella Remedy

Product NDC

43742-0163

11-digit product format

437420163

Labeler code

43742

Product ID

43742-0163_b8a1e265-9639-4287-b4d5-a8bb50d8623e

Type

HUMAN OTC DRUG

Nonproprietary name

Brucella Melitensis

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2012-09-28

Marketing end

2021-01-19

Substance

BRUCELLA MELITENSIS

Active strength

11 [hp_C]/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record