NDC 10544-179

Citalopram

Citalopram

Citalopram is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Blenheim Pharmacal, Inc.. The primary component is Citalopram Hydrobromide.

• Product ID: 10544-179_1360de1e-16e6-131a-e054-00144ff8d46c
• NDC: 10544-179
• Product Type: Human Prescription Drug
• Proprietary Name: Citalopram
• Generic Name: Citalopram
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2013-09-30
• Marketing Category: ANDA / ANDA
• Application Number: ANDA077045
• Labeler Name: Blenheim Pharmacal, Inc.
• Substance Name: CITALOPRAM HYDROBROMIDE
• Active Ingredient Strength: 20 mg/1
• Pharm Classes: Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10544-179-90

90 TABLET, FILM COATED in 1 BOTTLE (10544-179-90)

• Marketing Start Date: 2015-01-19
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10544-179-60 [10544017960]

Citalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA077045
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2015-02-11
• Inactivation Date: 2020-01-31

NDC 10544-179-90 [10544017990]

Citalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA077045
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2015-01-19
• Inactivation Date: 2020-01-31

NDC 10544-179-30 [10544017930]

Citalopram TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA077045
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2015-04-02
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
CITALOPRAM HYDROBROMIDE	20 mg/1

OpenFDA Data

• SPL SET ID: 5dcf0419-355b-4751-bf4c-2d45b1be93a6
• Manufacturer:
  • Blenheim Pharmacal, Inc.
• UNII:
  • I1E9D14F36
• RxNorm Concept Unique ID - RxCUI:
  • 309314
  • 200371
• UPC Code:
  • 0310544182309

Pharmacological Class

• Serotonin Reuptake Inhibitor [EPC]
• Serotonin Uptake Inhibitors [MoA]

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

NDC	Brand Name	Generic Name
0054-0062	Citalopram	Citalopram
0121-0848	Citalopram	Citalopram Hydrobromide
0121-1696	Citalopram	Citalopram Hydrobromide
0185-0371	Citalopram	Citalopram Hydrobromide
0185-0372	Citalopram	Citalopram Hydrobromide
0185-0373	Citalopram	Citalopram Hydrobromide
0378-6231	Citalopram	citalopram
0378-6232	Citalopram	citalopram
0378-6233	Citalopram	citalopram
0615-6510	Citalopram	Citalopram
0615-6511	Citalopram	Citalopram
0615-6512	Citalopram	Citalopram
0615-8022	Citalopram	Citalopram Hydrobromide
0615-8023	Citalopram	Citalopram Hydrobromide
0615-8141	Citalopram	Citalopram Hydrobromide
0713-4740	Citalopram	Citalopram Tablets
0713-4741	Citalopram	Citalopram Tablet
68071-1970	Citalopram	Citalopram
68071-3042	Citalopram	Citalopram
68071-3034	Citalopram	Citalopram
68071-3357	Citalopram	Citalopram
68071-4291	Citalopram	Citalopram
68071-4604	Citalopram	Citalopram
68071-4477	Citalopram	Citalopram
68071-4324	Citalopram	Citalopram
68084-737	Citalopram	Citalopram
68084-744	Citalopram	Citalopram
68788-6810	Citalopram	Citalopram
68788-0005	Citalopram	Citalopram
68788-0007	Citalopram	Citalopram
69097-822	Citalopram	Citalopram
69097-824	Citalopram	Citalopram
69097-823	Citalopram	Citalopram
70518-0449	Citalopram	Citalopram
70518-0561	Citalopram	Citalopram
71335-0541	Citalopram	Citalopram
71335-0573	Citalopram	Citalopram
71335-0712	Citalopram	Citalopram
71335-0656	Citalopram	Citalopram
0713-4742	Citalopram	Citalopram
10544-149	Citalopram	Citalopram
10544-179	Citalopram	Citalopram
10544-006	Citalopram	Citalopram
10544-150	Citalopram	Citalopram
10544-182	Citalopram	Citalopram
13107-005	Citalopram	Citalopram
13107-007	Citalopram	Citalopram
13107-006	Citalopram	Citalopram
21695-031	Citalopram	Citalopram
21695-032	Citalopram	Citalopram