Atropine SulfateInjection, USP
- Preservative-free
- Vial closure is not made with natural rubber latex
- This drug product is not FDA-approved
- These marketed unapproved Atropine products have been replaced with NDC 0157-1004-25 and 0517-1001-25. All future orders will be filled with FDA-approved Atropine NDC 0517-1004-25 and 0517-1001-25. Marketed unapproved Atropine (NDC 0517-0401-25 and 05171010-25) can remain in your inventory. There is no need to return the product, and they are suitable for use through expiry unless a situation arises to warrant a return.
For more information on FDA-approved Atropine Sulfate Injection, USP click here.
Pack NDC# | Strength | Supplied As | Shelf Pack | Vial Opening Size | Product Info | Availability | ||
---|---|---|---|---|---|---|---|---|
Strength:
0.4 mg/mL Supplied As:1 mL |
0517-0401-25 |
0.4 mg/mL |
1 mL |
25 | 13 mm | Product Label Full Prescribing Information Safety Data Sheet | Discontinued | |
Product Label Full Prescribing Information Safety Data Sheet Wholesaler Numbers
Case Information
|
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Strength:
1 mg/mL Supplied As:1 mL |
0517-1010-25 |
1 mg/mL |
1 mL |
25 | 13 mm | Product Label Full Prescribing Information Safety Data Sheet | Discontinued | |
Product Label Full Prescribing Information Safety Data Sheet Wholesaler Numbers
Case Information
|
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