Chlorpromazine Hydrochloride 00832-6019-01

Package NDC

00832-6019-01

Manufacturer: Upsher-Smith Laboratories, Llc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 3, 2011
Listing Expires: December 31, 2027
Application: ANDA084113

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Active Ingredients

Ingredient	Strength
Chlorpromazine Hydrochloride	50 mg/1

Drug Class

Phenothiazine [EPC]Phenothiazines [CS]

Selected Package

00832-6019-01Selected

1 BLISTER PACK in 1 CARTON (0832-6019-01) / 100 TABLET, FILM COATED in 1 BLISTER PACK (0832-6019-89)

Other packages for this product(2)

00832-6019-00

100 TABLET, FILM COATED in 1 BOTTLE (0832-6019-00)

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00832-6019-10

1000 TABLET, FILM COATED in 1 BOTTLE (0832-6019-10)

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