NDC 62980-515

Ranitidine 300 mg

Ranitidine

Ranitidine 300 mg is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Vivimed Labs Limited. The primary component is Ranitidine Hydrochloride.

• Product ID: 62980-515_66489df3-56c1-4b61-b8a4-f8c2a49f4341
• NDC: 62980-515
• Product Type: Human Prescription Drug
• Proprietary Name: Ranitidine 300 mg
• Generic Name: Ranitidine
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2019-04-01
• Marketing Category: ANDA / ANDA
• Application Number: ANDA210010
• Labeler Name: Vivimed Labs Limited
• Substance Name: RANITIDINE HYDROCHLORIDE
• Active Ingredient Strength: 300 mg/1
• Pharm Classes: Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 62980-515-05

35 TABLET, FILM COATED in 1 CARTON (62980-515-05)

• Marketing Start Date: 2019-04-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 62980-515-02 [62980051502]

Ranitidine 300 mg TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA210010
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-04-01
• Marketing End Date: 2019-11-26

NDC 62980-515-01 [62980051501]

Ranitidine 300 mg TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA210010
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-04-01
• Marketing End Date: 2019-11-26

NDC 62980-515-03 [62980051503]

Ranitidine 300 mg TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA210010
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-04-01
• Marketing End Date: 2019-11-26

NDC 62980-515-05 [62980051505]

Ranitidine 300 mg TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA210010
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-04-01
• Marketing End Date: 2019-11-26

Drug Details

Active Ingredients

Ingredient	Strength
RANITIDINE HYDROCHLORIDE	300 mg/1

OpenFDA Data

• SPL SET ID: bbf8c05d-0c45-4d6c-a787-41452d35fda8
• Manufacturer:
  • Vivimed Labs Limited
• UNII:
  • BK76465IHM
• RxNorm Concept Unique ID - RxCUI:
  • 198193
  • 198191

Pharmacological Class

• Histamine H2 Receptor Antagonists [MoA]
• Histamine-2 Receptor Antagonist [EPC]

NDC Crossover Matching brand name "Ranitidine 300 mg" or generic name "Ranitidine"

NDC	Brand Name	Generic Name
62980-515	Ranitidine 300 mg	Ranitidine 300 mg
10202-852	7 Select Acid Reducer	Ranitidine
0904-6350	Acid Reducer	Ranitidine
0113-7950	basic care acid reducer	Ranitidine
0113-7852	basic care acid reducer 150	Ranitidine
0113-7876	basic care acid reducer 75	Ranitidine
0113-0852	Good Sense Acid Reducer	Ranitidine
0113-0876	Good Sense Acid Reducer	Ranitidine
10202-712	MAXIMUM STRENGTH RANITIDINE	Ranitidine
0597-0121	Maximum Strength Zantac	ranitidine
0121-0727	Ranitidine	RANITIDINE
0121-4727	Ranitidine	RANITIDINE
0172-4357	Ranitidine	Ranitidine
0172-4358	Ranitidine	Ranitidine
0363-0352	Ranitidine	Ranitidine
0440-8300	Ranitidine	Ranitidine
0440-8305	Ranitidine	Ranitidine
0615-4513	Ranitidine	Ranitidine
0615-4514	Ranitidine	Ranitidine
0615-8021	Ranitidine	Ranitidine
0781-6087	Ranitidine	Ranitidine
0904-6349	Ranitidine	Ranitidine
0904-6716	Ranitidine	Ranitidine
0904-6921	Ranitidine	Ranitidine
10544-056	Ranitidine	Ranitidine
10544-438	Ranitidine	Ranitidine
10544-516	Ranitidine	Ranitidine
11673-849	Ranitidine	Ranitidine
0904-6715	ranitidine 75	Ranitidine
11673-023	up and up ranitidine	Ranitidine
0363-0852	wal zan 150	Ranitidine
0363-0950	wal zan 150	Ranitidine
0363-1876	wal zan 75	Ranitidine
0363-0362	Wal-Zan	Ranitidine
0597-0122	Zantac 75	ranitidine
0597-0120	Zantac Maximum Strength 150 Cool Mint	ranitidine