Propranolol Hcl And Hydrochlorothiazide

   
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Propranolol Hcl And Hydrochlorothiazide


Drug - Propranolol Hcl And Hydrochlorothiazide
The trade name of the product as shown on the labeling.

Dosage - TABLET; ORAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Hydrochlorothiazide; Propranolol Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 25MG;80MG
The potency of the active ingredient(s), Hydrochlorothiazide; Propranolol Hydrochloride. May repeat for multiple part products.

Applicant - PUREPAC PHARM
The firm name holding legal responsibility for Propranolol Hcl And Hydrochlorothiazide. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 070852
The FDA assigned number to Propranolol Hcl And Hydrochlorothiazide. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Propranolol Hcl And Hydrochlorothiazide. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

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

Approval Date - May 15, 1986
The date Propranolol Hcl And Hydrochlorothiazide 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 Propranolol Hcl And Hydrochlorothiazide. 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 Propranolol Hcl And Hydrochlorothiazide is in. Format is RX, OTC, DISCN.

Applicant Full Name - Purepac Pharmaceutical Co
The full name of the firm holding legal responsibility for the new application of Propranolol Hcl And Hydrochlorothiazide.

Propranolol Hcl And Hydrochlorothiazide