NDC 53489-281

Ergoloid Mesylates

Dihydroergocornine Mesylate, Dihydroergocristine Mesylate, Dihydro-.alpha.-ergocryptine Mesylate, And Dihydro-.beta.-ergocryptine Mesylate

Ergoloid Mesylates is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is Dihydroergocornine Mesylate; Dihydroergocristine Mesylate; Dihydro-.alpha.-ergocryptine Mesylate; Dihydro-.beta.-ergocryptine Mesylate.

• Product ID: 53489-281_273c1270-5303-44f5-be30-0c779d88fea1
• NDC: 53489-281
• Product Type: Human Prescription Drug
• Proprietary Name: Ergoloid Mesylates
• Generic Name: Dihydroergocornine Mesylate, Dihydroergocristine Mesylate, Dihydro-.alpha.-ergocryptine Mesylate, And Dihydro-.beta.-ergocryptine Mesylate
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 1991-10-31
• Marketing Category: ANDA / ANDA
• Application Number: ANDA081113
• Labeler Name: Sun Pharmaceutical Industries, Inc.
• Substance Name: DIHYDROERGOCORNINE MESYLATE; DIHYDROERGOCRISTINE MESYLATE; DIHYDRO-.ALPHA.-ERGOCRYPTINE MESYLATE; DIHYDRO-.BETA.-ERGOCRYPTINE MESYLATE
• Active Ingredient Strength: 0 mg/1; mg/1; mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 53489-281-01

100 TABLET in 1 BOTTLE, PLASTIC (53489-281-01)

• Marketing Start Date: 1991-10-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 53489-281-01 [53489028101]

Ergoloid Mesylates TABLET

• Marketing Category: ANDA
• Application Number: ANDA081113
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1991-10-31

NDC 53489-281-05 [53489028105]

Ergoloid Mesylates TABLET

• Marketing Category: ANDA
• Application Number: ANDA081113
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1991-10-31

NDC 53489-281-02 [53489028102]

Ergoloid Mesylates TABLET

• Marketing Category: ANDA
• Application Number: ANDA081113
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1991-10-31

NDC 53489-281-10 [53489028110]

Ergoloid Mesylates TABLET

• Marketing Category: ANDA
• Application Number: ANDA081113
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1991-10-31

NDC 53489-281-03 [53489028103]

Ergoloid Mesylates TABLET

• Marketing Category: ANDA
• Application Number: ANDA081113
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1991-10-31

Drug Details

Active Ingredients

Ingredient	Strength
DIHYDROERGOCORNINE MESYLATE	.333 mg/1

OpenFDA Data

• SPL SET ID: cf973160-d467-4192-a432-04c8c2140369
• Manufacturer:
  • Sun Pharmaceutical Industries, Inc.
• UNII:
  • 42RX8KPW29
  • Z4I7BU58DN
  • DS7CL18UAM
  • 79Y4U49I29
• RxNorm Concept Unique ID - RxCUI:
  • 318179
• UPC Code:
  • 0353489281010

Medicade Reported Pricing

53489028101 ERGOLOID MESYLATES 1 MG TAB

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Ergoloid Mesylates" or generic name "Dihydroergocornine Mesylate, Dihydroergocristine Mesylate, Dihydro-.alpha.-ergocryptine Mesylate, And Dihydro-.beta.-ergocryptine Mesylate"

NDC	Brand Name	Generic Name
53489-281	Ergoloid Mesylates	Dihydroergocornine Mesylate, Dihydroergocristine Mesylate, Dihydro-.alpha.-ergocryptine mesylate, and Dihydro-.beta.-ergocryptine mesylate
68151-2780	Ergoloid Mesylates	Dihydroergocornine Mesylate, Dihydroergocristine Mesylate, Dihydro-.alpha.-ergocryptine mesylate, and Dihydro-.beta.-ergocryptine mesylate