Atropine Sulfate Ansyr Plastic Syringe

   
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Atropine Sulfate Ansyr Plastic Syringe


Drug - Atropine Sulfate Ansyr Plastic Syringe
The trade name of the product as shown on the labeling.

Dosage - INJECTABLE; IM-IV-SC
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Atropine Sulfate
Multiple ingredients are in alphabetical order.

Strength - 0.05MG/ML
The potency of the active ingredient(s), Atropine Sulfate. May repeat for multiple part products.

Applicant - HOSPIRA
The firm name holding legal responsibility for Atropine Sulfate Ansyr Plastic Syringe. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 021146
The FDA assigned number to Atropine Sulfate Ansyr Plastic Syringe. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Atropine Sulfate Ansyr Plastic Syringe. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code -
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Jul 9, 2001
The date Atropine Sulfate Ansyr Plastic Syringe was approved as stated in the FDA approval letter to the applicant. The format is Mmm dd, yyyy. Products approved prior to the January 1, 1982 contain the phrase: "Approved prior to Jan 1, 1982".

Reference Listed Drug (RLD) - No
The pioneer or innovator of Atropine Sulfate Ansyr Plastic Syringe. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - RX
The group or category of approved drugs Atropine Sulfate Ansyr Plastic Syringe is in. Format is RX, OTC, DISCN.

Applicant Full Name - Hospira Inc
The full name of the firm holding legal responsibility for the new application of Atropine Sulfate Ansyr Plastic Syringe.

Atropine Sulfate Ansyr Plastic Syringe