NDC 0378-0150

Chlorothiazide

Chlorothiazide

Chlorothiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Mylan Pharmaceuticals Inc.. The primary component is Chlorothiazide.

• Product ID: 0378-0150_4f2271f7-98bc-4b5c-acc6-ad65a717ac84
• NDC: 0378-0150
• Product Type: Human Prescription Drug
• Proprietary Name: Chlorothiazide
• Generic Name: Chlorothiazide
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 1975-06-26
• Marketing End Date: 2020-12-31
• Marketing Category: ANDA / ANDA
• Application Number: ANDA084217
• Labeler Name: Mylan Pharmaceuticals Inc.
• Substance Name: CHLOROTHIAZIDE
• Active Ingredient Strength: 250 mg/1
• Pharm Classes: Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
• NDC Exclude Flag: N

Packaging

NDC 0378-0150-01

100 TABLET in 1 BOTTLE, PLASTIC (0378-0150-01)

• Marketing Start Date: 1975-06-26
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0378-0150-01 [00378015001]

Chlorothiazide TABLET

• Marketing Category: ANDA
• Application Number: ANDA084217
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1975-06-26
• Marketing End Date: 2020-12-31

Drug Details

Active Ingredients

Ingredient	Strength
CHLOROTHIAZIDE	250 mg/1

OpenFDA Data

• SPL SET ID: d652ef6f-2112-43ea-ba01-c3bf4f8d8030
• Manufacturer:
  • Mylan Pharmaceuticals Inc.
• UNII:
  • 77W477J15H
• RxNorm Concept Unique ID - RxCUI:
  • 197475
  • 197476
• UPC Code:
  • 0303780376687

Pharmacological Class

• Increased Diuresis [PE]
• Thiazide Diuretic [EPC]
• Thiazides [CS]

NDC Crossover Matching brand name "Chlorothiazide" or generic name "Chlorothiazide"

NDC	Brand Name	Generic Name
0143-1209	Chlorothiazide	Chlorothiazide
0143-1210	Chlorothiazide	Chlorothiazide
0378-0150	Chlorothiazide	chlorothiazide
0378-0162	Chlorothiazide	chlorothiazide
63323-658	Chlorothiazide	CHLOROTHIAZIDE SODIUM
65649-311	DIURIL	CHLOROTHIAZIDE