NDC 68788-6810

Citalopram

Citalopram

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

• Product ID: 68788-6810_ca87bc78-17c8-4b52-867a-ca3f71277acd
• NDC: 68788-6810
• Product Type: Human Prescription Drug
• Proprietary Name: Citalopram
• Generic Name: Citalopram
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2016-11-07
• Marketing Category: ANDA / ANDA
• Application Number: ANDA077289
• Labeler Name: Preferred Pharmaceuticals Inc.
• Substance Name: CITALOPRAM HYDROBROMIDE
• Active Ingredient Strength: 10 mg/1
• Pharm Classes: Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 68788-6810-6

60 TABLET in 1 BOTTLE (68788-6810-6)

• Marketing Start Date: 2016-11-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68788-6810-1 [68788681001]

Citalopram TABLET

• Marketing Category: ANDA
• Application Number: ANDA077289
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-11-07
• Marketing End Date: 2019-07-30

NDC 68788-6810-6 [68788681006]

Citalopram TABLET

• Marketing Category: ANDA
• Application Number: ANDA077289
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-11-07
• Marketing End Date: 2019-07-30

NDC 68788-6810-8 [68788681008]

Citalopram TABLET

• Marketing Category: ANDA
• Application Number: ANDA077289
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-11-07
• Marketing End Date: 2019-07-30

NDC 68788-6810-3 [68788681003]

Citalopram TABLET

• Marketing Category: ANDA
• Application Number: ANDA077289
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-11-07
• Marketing End Date: 2019-07-30

NDC 68788-6810-9 [68788681009]

Citalopram TABLET

• Marketing Category: ANDA
• Application Number: ANDA077289
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2016-11-07
• Marketing End Date: 2019-07-30

Drug Details

Active Ingredients

Ingredient	Strength
CITALOPRAM HYDROBROMIDE	10 mg/1

OpenFDA Data

• SPL SET ID: 702c58a6-24a8-4ece-8d10-46950b01cad0
• Manufacturer:
  • Preferred Pharmaceuticals Inc.
• UNII:
  • I1E9D14F36
• RxNorm Concept Unique ID - RxCUI:
  • 283672

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