NDC 21695-880

Methyldopa

Methyldopa

Methyldopa is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Rebel Distributors Corp. The primary component is Methyldopa.

• Product ID: 21695-880_cf051ddf-aca5-4bdc-ac16-27310d5fd59a
• NDC: 21695-880
• Product Type: Human Prescription Drug
• Proprietary Name: Methyldopa
• Generic Name: Methyldopa
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 1984-02-20
• Marketing Category: ANDA / ANDA
• Application Number: ANDA070343
• Labeler Name: Rebel Distributors Corp
• Substance Name: METHYLDOPA
• Active Ingredient Strength: 500 mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 21695-880-60

60 TABLET, FILM COATED in 1 BOTTLE (21695-880-60)

• Marketing Start Date: 1984-02-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 21695-880-60 [21695088060]

Methyldopa TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA070343
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1984-02-20
• Inactivation Date: 2019-09-24

Drug Details

Active Ingredients

Ingredient	Strength
METHYLDOPA	500 mg/1

OpenFDA Data

• SPL SET ID: 60a57abf-9487-4093-9709-40f05755e7b1
• Manufacturer:
  • Rebel Distributors Corp
• UNII:
  • 56LH93261Y
• RxNorm Concept Unique ID - RxCUI:
  • 197956
  • 197958

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

NDC	Brand Name	Generic Name
0378-0421	Methyldopa	methyldopa
0378-0611	Methyldopa	methyldopa
16729-030	Methyldopa	Methyldopa
16729-031	Methyldopa	Methyldopa
21695-879	Methyldopa	Methyldopa
21695-880	Methyldopa	Methyldopa
42254-351	Methyldopa	Methyldopa
51079-200	Methyldopa	methyldopa
51079-201	Methyldopa	methyldopa
62135-321	Methyldopa	Methyldopa
62135-322	Methyldopa	Methyldopa
68151-2791	Methyldopa	Methyldopa