NDC 68788-0007

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: 68788-0007_f3013718-656d-4a5c-8f22-4900d5777407
• NDC: 68788-0007
• Product Type: Human Prescription Drug
• Proprietary Name: Citalopram
• Generic Name: Citalopram
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2014-10-17
• Marketing Category: ANDA / ANDA
• Application Number: ANDA077534
• Labeler Name: Preferred Pharmaceuticals, Inc.
• Substance Name: CITALOPRAM HYDROBROMIDE
• Active Ingredient Strength: 40 mg/1
• Pharm Classes: Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 68788-0007-6

60 TABLET in 1 BOTTLE (68788-0007-6)

• Marketing Start Date: 2014-10-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68788-0007-1 [68788000701]

Citalopram TABLET

• Marketing Category: ANDA
• Application Number: ANDA077534
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-10-17
• Marketing End Date: 2019-07-30

NDC 68788-0007-3 [68788000703]

Citalopram TABLET

• Marketing Category: ANDA
• Application Number: ANDA077534
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-10-17
• Marketing End Date: 2019-07-30

NDC 68788-0007-9 [68788000709]

Citalopram TABLET

• Marketing Category: ANDA
• Application Number: ANDA077534
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-10-17
• Marketing End Date: 2019-07-30

NDC 68788-0007-8 [68788000708]

Citalopram TABLET

• Marketing Category: ANDA
• Application Number: ANDA077534
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-10-17
• Marketing End Date: 2019-07-30

NDC 68788-0007-6 [68788000706]

Citalopram TABLET

• Marketing Category: ANDA
• Application Number: ANDA077534
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-10-17
• Marketing End Date: 2019-07-30

Drug Details

Active Ingredients

Ingredient	Strength
CITALOPRAM HYDROBROMIDE	40 mg/1

OpenFDA Data

• SPL SET ID: 22e98bda-195f-4301-b0ea-ae99edf68ed5
• Manufacturer:
  • Preferred Pharmaceuticals, Inc.
• UNII:
  • I1E9D14F36
• RxNorm Concept Unique ID - RxCUI:
  • 309314

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