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Tetracycline Hydrochloride - 55289-256-12 - (Tetracycline Hydrochloride)

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Drug Information of Tetracycline Hydrochloride

Product NDC: 55289-256
Proprietary Name: Tetracycline Hydrochloride
Non Proprietary Name: Tetracycline Hydrochloride
Active Ingredient(s): 250    mg/1 & nbsp;   Tetracycline Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Tetracycline Hydrochloride

Product NDC: 55289-256
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA060704
Marketing Category: ANDA
Start Marketing Date: 20100323

Package Information of Tetracycline Hydrochloride

Package NDC: 55289-256-12
Package Description: 12 CAPSULE in 1 BOTTLE, PLASTIC (55289-256-12)

NDC Information of Tetracycline Hydrochloride

NDC Code 55289-256-12
Proprietary Name Tetracycline Hydrochloride
Package Description 12 CAPSULE in 1 BOTTLE, PLASTIC (55289-256-12)
Product NDC 55289-256
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tetracycline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100323
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name TETRACYCLINE HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Antimicrobial [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Tetracycline Hydrochloride


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