Federal Register - October 20, 2021

Versión en texto ¿Qué es?Dateas es un sitio independiente no afiliado a entidades gubernamentales. La fuente de los documentos PDF aquí publicados es la entidad gubernamental indicada en cada uno de ellos. Las versiones en texto son transcripciones no oficiales que realizamos para facilitar el acceso y la búsqueda de información, pero pueden contener errores o no estar completas.

Fuente: Federal Register

57996

Federal Register / Vol. 86, No. 200 / Wednesday, October 20, 2021 / Rules and Regulations Drug labeler code
Firm name and address

2
Drug labeler code
Firm name and address

065085

Piramal Pharma Ltd., Ground Floor, Piramal Ananta, Agastya Corporate Park, Mumbai, Maharashtra, 400070, India

069043

Cronus Pharma Specialities India Private Ltd., Sy No99/1, M/s GMR Hyderabad Aviation SEZ Ltd., Mamidipalli Village, Shamshabad Mandal, Ranga Reddy, Hyderabad, Telangana, 501218, India

086121

Anivive Lifesciences, Inc., 3250 Airflite Way, Suite 400, Long Beach, CA 90807

PART 516NEW ANIMAL DRUGS FOR
MINOR USE AND MINOR SPECIES
3. The authority citation for part 516
continues to read as follows:

Authority: 21 U.S.C. 360ccc, 360ccc2, 371.

4. Add 516.1858 to subpart E to read as follows:

516.1858

Potassium bromide.

a Specifications. Each chewable tablet contains 250 or 500 milligrams mg potassium bromide.
b Sponsor. See No. 055246 in 510.600c of this chapter.
c Conditions of use1 Amount.
Administer 25 to 68 mg per kilogram 11
to 31 mg per pound of body weight once daily. The dosage can be divided and should be adjusted to clinical response.
2 Indications for use. For the control of seizures associated with idiopathic epilepsy in dogs.
3 Limitations. Federal law restricts this drug to use by or on the order of a licensed veterinarian. It is a violation of Federal law to use this product other than as directed in the labeling.
5. Add 516.2980 to subpart E to read as follows:

lotter on DSK11XQN23PROD with RULES1

516.2980

Verdinexor.

a Specifications. Each tablet contains 2.5, 10, or 50 milligrams mg verdinexor.
b Sponsor. See No. 086121 in 510.600c of this chapter.
c Conditions of use1 Amount.
Administer verdinexor tablets orally at an initial dose of 1.25 mg per kilogram mg/kg of body weight twice per week with at least 72 hours between doses. If tolerated after 2 weeks, increase the
VerDate Sep<11>2014

16:22 Oct 19, 2021

Jkt 256001

dose to 1.5 mg/kg twice per week with at least 72 hours between doses.
2 Indications for use. For the treatment of lymphoma in dogs.
3 Limitations. Federal law restricts this drug to use by or on the order of a licensed veterinarian. It is a violation of Federal law to use this product other than as directed in the labeling.
PART 520ORAL DOSAGE FORM
NEW ANIMAL DRUGS
6. The authority citation for part 520
continues to read as follows:

Authority: 21 U.S.C. 360b.

7. In 520.441, revise paragraph b1
to read as follows:

520.441

Chlortetracycline powder.

b
1 Nos. 000010, 054771, and 069254
for use as in paragraph d of this section.

8. In 520.455, revise the section heading and paragraph b to read as follows:
520. 455

Clomipramine.

b Sponsors. See Nos. 051311 and 086039 in 510.600c of this chapter.

9. In 520.905c, revise paragraph e2 to read as follows:
520.905c
Fenbendazole paste.

e
2 Beef and dairy cattlei Amount.
Administer orally 2.3 mg/lb 5 mg/kg body weight.

PO 00000

Frm 00012

Fmt 4700

Sfmt 4700

ii Indications for use. For the treatment and control of: Lungworms:
Adult Dictyocaulus viviparus;
Stomach worms: Adult brown stomach worms Ostertagia ostertagi, adult and fourth-stage larvae barberpole worms Haemonchus contortus, fourth-stage larvae barberpole worms H. placei, and adult and fourth-stage larvae small stomach worms Trichostrongylus axei;
Intestinal worms adult and fourth-stage larvae: Hookworms Bunostomum phlebotomum, thread-necked intestinal worms Nematodirus helvetianus, small intestinal worms Cooperia punctata and C. oncophora, bankrupt worms Trichostrongylus colubriformis, and nodular worms Oesophagostomum radiatum.
iii Limitations. Milk taken during treatment and for 96 hours after the last treatment must not be used for human consumption. Cattle must not be slaughtered for human consumption within 8 days following last treatment with this drug product. Not for use in beef calves less than 2 months of age, dairy calves, and veal calves. A
withdrawal period has not been established for this product in preruminating calves.
10. In 520.1189, revise paragraph b to read as follows:
520.1189

Itraconazole.

b Sponsor. See No. 051311 in 510.600c of this chapter.

11. In 520.1248, revise paragraphs b and c1 to read as follows:
520.1248

Levothyroxine.

E:FRFM20OCR1.SGM

20OCR1

Acerca de esta edición

Federal Register - October 20, 2021

TítuloFederal Register

PaísEstados Unidos de América

Fecha20/10/2021

Nro. de páginas226

Nro. de ediciones7805

Primera edición14/03/1936

Ultima edición30/06/2026

Descargar esta edición

Otras ediciones

<<<Octubre 2021>>>
DLMMJVS
12
3456789
10111213141516
17181920212223
24252627282930
31