Minocycline Hydrochloride 72789-0530

Product NDC

72789-0530

Manufacturer: Pd-Rx Pharmaceuticals, Inc.
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: September 30, 2016
Listing Expires: December 31, 2026
Application: ANDA204453

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Active Ingredients

Ingredient	Strength
Minocycline Hydrochloride	135 mg/1

Drug Class

Decreased Prothrombin Activity [PE]Tetracycline-class Drug [EPC]Tetracyclines [CS]

Packaging Options(1)

72789-0530-30

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-530-30)

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