NDC 68071-1973

Lovastatin

Lovastatin

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

• Product ID: 68071-1973_4925f194-c8e0-242c-e054-00144ff88e88
• NDC: 68071-1973
• Product Type: Human Prescription Drug
• Proprietary Name: Lovastatin
• Generic Name: Lovastatin
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2001-12-17
• Marketing Category: ANDA / ANDA
• Application Number: ANDA075636
• Labeler Name: NuCare Pharmaceuticals, Inc.
• Substance Name: LOVASTATIN
• Active Ingredient Strength: 10 mg/1
• Pharm Classes: HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 68071-1973-6

60 TABLET in 1 BOTTLE (68071-1973-6)

• Marketing Start Date: 2017-02-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68071-1973-9 [68071197309]

Lovastatin TABLET

• Marketing Category: ANDA
• Application Number: ANDA075636
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-02-22
• Marketing End Date: 2018-12-31

NDC 68071-1973-6 [68071197306]

Lovastatin TABLET

• Marketing Category: ANDA
• Application Number: ANDA075636
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-02-22
• Marketing End Date: 2018-12-31

NDC 68071-1973-3 [68071197303]

Lovastatin TABLET

• Marketing Category: ANDA
• Application Number: ANDA075636
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-02-22
• Marketing End Date: 2018-12-31

NDC 68071-1973-8 [68071197308]

Lovastatin TABLET

• Marketing Category: ANDA
• Application Number: ANDA075636
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-02-22
• Marketing End Date: 2018-12-31

Drug Details

Active Ingredients

Ingredient	Strength
LOVASTATIN	10 mg/1

OpenFDA Data

• SPL SET ID: 4925f194-c923-242c-e054-00144ff88e88
• Manufacturer:
  • NuCare Pharmaceuticals, Inc.
• UNII:
  • 9LHU78OQFD
• RxNorm Concept Unique ID - RxCUI:
  • 197903

Pharmacological Class

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

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

NDC	Brand Name	Generic Name
0093-0576	Lovastatin	Lovastatin
0093-0926	Lovastatin	Lovastatin
0093-0928	Lovastatin	Lovastatin
0185-0070	Lovastatin	Lovastatin
0185-0072	Lovastatin	Lovastatin
0185-0074	Lovastatin	Lovastatin
0440-6694	Lovastatin	Lovastatin
0615-5589	Lovastatin	Lovastatin
0615-6551	Lovastatin	Lovastatin
0615-6590	Lovastatin	Lovastatin
0615-7674	Lovastatin	Lovastatin
0615-7679	Lovastatin	Lovastatin
0615-7685	Lovastatin	Lovastatin
0615-7690	Lovastatin	Lovastatin
0615-8151	Lovastatin	lovastatin
0615-8152	Lovastatin	lovastatin
10544-235	Lovastatin	Lovastatin
10544-241	Lovastatin	Lovastatin
10544-242	Lovastatin	Lovastatin
10544-246	Lovastatin	Lovastatin
21695-534	Lovastatin	Lovastatin
21695-535	Lovastatin	Lovastatin
21695-536	Lovastatin	Lovastatin
33261-547	Lovastatin	Lovastatin
33261-548	Lovastatin	Lovastatin
33261-549	Lovastatin	Lovastatin
35356-885	Lovastatin	Lovastatin
42254-025	Lovastatin	Lovastatin
42254-028	Lovastatin	Lovastatin
42254-106	Lovastatin	Lovastatin
68001-224	Lovastatin	Lovastatin
68001-315	Lovastatin	Lovastatin
68001-316	Lovastatin	Lovastatin
68001-214	Lovastatin	Lovastatin
68001-314	Lovastatin	Lovastatin
68071-3108	Lovastatin	Lovastatin
68071-1973	Lovastatin	Lovastatin
68071-3127	Lovastatin	Lovastatin
68071-3261	Lovastatin	Lovastatin
68071-3397	Lovastatin	Lovastatin
68071-4271	Lovastatin	Lovastatin
68084-559	Lovastatin	Lovastatin
68180-468	Lovastatin	Lovastatin
68180-467	Lovastatin	Lovastatin
68180-469	Lovastatin	Lovastatin
68645-576	Lovastatin	Lovastatin
68645-566	Lovastatin	Lovastatin
68788-2634	Lovastatin	Lovastatin
68645-567	Lovastatin	Lovastatin
68788-0926	Lovastatin	Lovastatin