Oxytetracycline Hydrochloride Powder
FDA Label NDC 24507-003

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Hebei Shengxue Dacheng Pharmaceutical Company, Ltd. for the product Oxytetracycline Hydrochloride (NDC 24507-003). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding oxytetracycline hydrochloride, usp, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Oxytetracycline Hydrochloride, Usp

25kg/DRUM LABEL

OXYTETRACYCLINE HYDROCHLORIDE

USP

Batch No.      Packing: 25kg/DRUM

MFG. Date       Gross Weight:

Retest Date:       Net Weight:

Storage: Store in an airtight container, protected from light, at or below
30° C, with excursions permitted up to 40° C.

Caution: For manufacturing, processing, or repacking.

Attention: Desiccant bag is placed inside of the aluminum bag.

MADE IN CHINA

Hebei Shengxue Dacheng Pharmaceutical Co.,Ltd.

NO.50 Shengxue Road Luancheng Shijiazhuang 051430 China

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