Ampicillin Injection, Powder, For Solution
Product Images NDC 83270-312

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Ampicillin (NDC 83270-312). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Onesource Specialty Pharma Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

1-g-carton (1gm Carton)

Ampicillin for Injection, USP 1 gram vial carton label with dimensions 136 x 56 x 66 mm. The label states the product is for intramuscular or intravenous use, sterile, and packaged in 10 vials of 1 gram each. The labeler is Onesource Specialty Pharma Limited. The packaging includes barcodes and directions for storage and use.*

FDA Label Image

1-g-vial (1gm Vial)

Ampicillin 1 gram per vial injection powder label for solution, USP. For intramuscular or intravenous use, sterile, prescription only. Label indicates ampicillin sodium equivalent content and dosage instructions. Manufactured by OneSource Specialty Pharma Limited, India. Includes storage instructions and barcode.*

FDA Label Image

250 mg-carton (250mg Carton)

Ampicillin for Injection, USP 250 mg/vial in a carton label from Onesource Specialty Pharma Limited. The label indicates the dosage form as injection powder for solution, suitable for intramuscular or intravenous use. The carton size is 136 x 56 x 66 mm, containing 10 vials of 250 mg each. The label includes manufacturer information, dosage instructions, and storage details.*

FDA Label Image

250 mg-vial (250mg Vial)

Label for Ampicillin injection powder for solution, 250 mg per vial. The label specifies the product is for intramuscular or intravenous use, sterile, and prescription only. It is manufactured by OneSource Specialty Pharma Limited, Beta Lactam Division, Bengaluru, India.*

FDA Label Image

2g-carton (2gm Carton)

Packaging label for Ampicillin for Injection, 2 grams per vial, powder for solution. The label indicates the product is for intramuscular and intravenous use and is sterile. The labeler shown is Onesource Specialty Pharma Limited. The carton dimensions are 164 x 68 x 70 mm, and the package contains 10 vials of 2 grams each. The label includes barcodes and dosage strength information prominently.*

FDA Label Image

2g-vial (2gm Vial)

Ampicillin 2 grams per vial injection powder label for sterile intravenous or intramuscular use. The label displays the proprietary and generic name "Ampicillin, USP," strength as 2 grams per vial, intended for prescription human use. It includes manufacturer details, storage instructions, and says to use the solution within 1 hour after reconstitution. The labeler is OneSource Specialty Pharma Limited.*

FDA Label Image

500 mg-carton (500mg Carton)

Ampicillin for Injection, USP 500 mg/vial in powder form for solution, presented in a carton holding 10 vials. The label specifies use for intramuscular or intravenous administration, labeled by ONESOURCE SPECIALTY PHARMA LIMITED. The carton dimensions are 136 x 56 x 66 mm, with distinct barcode and usage instructions visible.*

FDA Label Image

500 mg-vial (500mg Vial)

Ampicillin 500 mg/vial injection powder for solution label. The vial is sterile and intended for intramuscular or intravenous use. Manufactured by OneSource Specialty Pharma Limited, Beta Lactam Division, Bengaluru, India. The label includes dosing and storage instructions, lot and expiration date fields, and a barcode.*

FDA Label Image

Structure (Image 01)

Chemical structure of Ampicillin, showing its molecular composition including a beta-lactam ring, amino group, and a carboxylate group attached to a phenyl ring and other functional groups.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.