Labetalol Hydrochloride 58657-0907

Product NDC

58657-0907

Manufacturer: Method Pharmaceuticals, Llc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 1, 2025
Listing Expires: December 31, 2026
Application: ANDA075215

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Active Ingredients

Ingredient	Strength
Labetalol	200 mg/1

Drug Class

beta-Adrenergic Blocker [EPC]Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]

Packaging Options(1)

58657-0907-01

100 BLISTER PACK in 1 CARTON (58657-907-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (58657-907-10)

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