Neostigmine Methylsulfate Injection
Product Images NDC 51662-1557

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Neostigmine Methylsulfate (NDC 51662-1557). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Carton Inside Pouch (51662 1557 2 Box Labeling)

Neostigmine Methylsulfate Injection, USP is a prescription medicine used for intravenous use as a multiple dose vial. Each vial contains 10 mg of neostigmine which is equivalent to 1 mg/mL of the drug. Other ingredients include methylsulfate, phancol, sodium acetate trihydrate, and sodium chloride. The medicine should be protected from light and stored at controlled room temperature. The package insert contains instructions for use. Also available are the lot number and the NDC number 0548-9602-00.*

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Pouch Labeling (51662 1557 2 Pouch Labeling)

NEOSTIGMINE METHYLSULFATE INJECTION, USP is a prescription medication available in a 10mg per 10mL (1mg/mL) vial for intravenous use. The vial must be protected from light and stored between 68° to 77°F with permitted excursions to 15° to 30°C. The medication should be administered as per the manufacturer's package insert. The product is manufactured and distributed by HF Acquisition Co., LLC in Mukilteo, WA 98275.*

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Case Labeling (51662 1557 3 Case Labeling)

Neostigmine Methylsulfate Injection is a medication that comes in a box of 10 vials with 10mg of the active ingredient per 10mL vial. The medication is used to protect from light and to be stored between 68°F to 77°F, with excursions allowed between 59°F to 86°F. This medication is only for prescription use, and there are directions included in the manufacturer's package insert. The manufacturer of this medication is HF Acquisition Co., LLC and the original NDC number is 0548-9602-00.*

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Serialized Labeling (51662 1557 3 Serialized Labeling)

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Adverse 1 (Adverse 1)

Not available. The text seems to be incomplete and contains gibberish characters.*

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Adverse 2 (Adverse 2)

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Description (Description)

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How Supplied (How Supplied)

This text provides information about two different vial sizes of a medication with varying strengths measured in mg/mL. The first vial size contains 0.5 mg/mL and comes in packages of 10, while the second vial size contains 1 mg/mL and also comes in packages of 10. The medication's name is not given in this text.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.