NDC 68788-7193

Pravastatin sodium

Pravastatin Sodium

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

• Product ID: 68788-7193_77d581ee-7d09-4408-ab06-336c3a8e482e
• NDC: 68788-7193
• Product Type: Human Prescription Drug
• Proprietary Name: Pravastatin sodium
• Generic Name: Pravastatin Sodium
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2018-07-18
• Marketing Category: ANDA / ANDA
• Application Number: ANDA076714
• Labeler Name: Preferred Pharmaceuticals Inc.
• Substance Name: PRAVASTATIN SODIUM
• Active Ingredient Strength: 80 mg/1
• Pharm Classes: HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 68788-7193-3

30 TABLET in 1 BOTTLE (68788-7193-3)

• Marketing Start Date: 2018-07-18
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68788-7193-8 [68788719308]

Pravastatin sodium TABLET

• Marketing Category: ANDA
• Application Number: ANDA076714
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-07-18
• Marketing End Date: 2019-11-12

NDC 68788-7193-2 [68788719302]

Pravastatin sodium TABLET

• Marketing Category: ANDA
• Application Number: ANDA076714
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-07-18
• Marketing End Date: 2019-11-12

NDC 68788-7193-1 [68788719301]

Pravastatin sodium TABLET

• Marketing Category: ANDA
• Application Number: ANDA076714
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-07-18
• Marketing End Date: 2019-11-12

NDC 68788-7193-3 [68788719303]

Pravastatin sodium TABLET

• Marketing Category: ANDA
• Application Number: ANDA076714
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-07-18
• Marketing End Date: 2019-11-12

NDC 68788-7193-6 [68788719306]

Pravastatin sodium TABLET

• Marketing Category: ANDA
• Application Number: ANDA076714
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-07-18
• Marketing End Date: 2019-11-12

NDC 68788-7193-9 [68788719309]

Pravastatin sodium TABLET

• Marketing Category: ANDA
• Application Number: ANDA076714
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-07-18
• Marketing End Date: 2019-11-12

Drug Details

Active Ingredients

Ingredient	Strength
PRAVASTATIN SODIUM	80 mg/1

OpenFDA Data

• SPL SET ID: 77d581ee-7d09-4408-ab06-336c3a8e482e
• Manufacturer:
  • Preferred Pharmaceuticals Inc.
• UNII:
  • 3M8608UQ61
• RxNorm Concept Unique ID - RxCUI:
  • 904481

Pharmacological Class

• HMG-CoA Reductase Inhibitor [EPC]
• Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

NDC Crossover Matching brand name "Pravastatin sodium" or generic name "Pravastatin Sodium"

NDC	Brand Name	Generic Name
0093-0771	Pravastatin Sodium	Pravastatin Sodium
0093-7201	Pravastatin Sodium	Pravastatin Sodium
0093-7202	Pravastatin Sodium	Pravastatin Sodium
0093-7270	Pravastatin Sodium	Pravastatin Sodium
0615-6556	Pravastatin Sodium	Pravastatin Sodium
0615-6557	Pravastatin Sodium	Pravastain Sodium
0615-7740	Pravastatin Sodium	Pravastatin Sodium
0615-7868	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
0615-7869	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
0615-8029	Pravastatin Sodium	Pravastatin Sodium
0615-8030	Pravastatin Sodium	Pravastatin Sodium
68071-2088	Pravastatin Sodium	Pravastatin Sodium
68071-3247	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
68071-3253	pravastatin sodium	pravastatin sodium
68071-1917	Pravastatin sodium	Pravastatin sodium
68071-3358	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
68071-3361	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
68071-2194	Pravastatin sodium	Pravastatin sodium
68071-3366	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
68071-4039	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
68071-4707	pravastatin sodium	pravastatin sodium
68180-488	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
68180-487	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
68180-486	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
68180-485	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
68382-071	pravastatin sodium	pravastatin sodium
68382-070	pravastatin sodium	pravastatin sodium
68382-073	pravastatin sodium	pravastatin sodium
68382-072	pravastatin sodium	pravastatin sodium
68462-195	Pravastatin Sodium	Pravastatin Sodium
68462-198	Pravastatin Sodium	Pravastatin Sodium
68462-197	Pravastatin Sodium	Pravastatin Sodium
68462-196	Pravastatin Sodium	Pravastatin Sodium
68788-7253	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
68788-7013	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
68788-7193	Pravastatin sodium	Pravastatin sodium
68788-7316	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
68788-7413	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
69097-185	Pravastatin Sodium	Pravastatin Sodium
69097-186	Pravastatin Sodium	Pravastatin Sodium
69097-183	Pravastatin Sodium	Pravastatin Sodium
69097-184	Pravastatin Sodium	Pravastatin Sodium
70518-0304	Pravastatin Sodium	Pravastatin Sodium
70518-0412	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
70518-0549	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
70518-0707	pravastatin sodium	pravastatin sodium
70518-0423	Pravastatin Sodium	Pravastatin Sodium
70518-1197	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM
70518-0936	Pravastatin Sodium	Pravastatin Sodium
70518-1710	PRAVASTATIN SODIUM	PRAVASTATIN SODIUM