NDC 71610-371

Ranitidine Immediate release

Ranitidine

Ranitidine Immediate release is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Aphena Pharma Solutions - Tennessee, Llc. The primary component is Ranitidine Hydrochloride.

Product ID71610-371_d32add18-2d01-4d25-b3f0-07bf86a7c254
NDC71610-371
Product TypeHuman Prescription Drug
Proprietary NameRanitidine Immediate release
Generic NameRanitidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-08-22
Marketing CategoryANDA / ANDA
Application NumberANDA205512
Labeler NameAphena Pharma Solutions - Tennessee, LLC
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength300 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71610-371-80

180 TABLET in 1 BOTTLE (71610-371-80)
Marketing Start Date2019-12-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71610-371-80 [71610037180]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2019-12-05

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE300 mg/1

Pharmacological Class

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

NDC Crossover Matching brand name "Ranitidine Immediate release" or generic name "Ranitidine"

NDCBrand NameGeneric Name
70518-0004Ranitidine Immediate releaseRanitidine Immediate release
70518-0017Ranitidine Immediate releaseRanitidine Immediate release
70518-1043Ranitidine Immediate releaseRanitidine Immediate release
70518-1952Ranitidine Immediate releaseRanitidine Immediate release
71205-007Ranitidine Immediate releaseRanitidine Immediate release
71335-0042Ranitidine Immediate releaseRanitidine Immediate release
53002-1028Ranitidine Immediate releaseRanitidine Immediate release
58118-0803Ranitidine Immediate releaseRanitidine Immediate release
63187-855Ranitidine Immediate releaseRanitidine Immediate release
64380-804Ranitidine Immediate releaseRanitidine Immediate release
64380-803Ranitidine Immediate releaseRanitidine Immediate release
70934-332Ranitidine Immediate releaseRanitidine Immediate release
51407-244Ranitidine Immediate releaseRanitidine Immediate release
51407-245Ranitidine Immediate releaseRanitidine Immediate release
64380-937Ranitidine Immediate releaseRanitidine Immediate release
64380-936Ranitidine Immediate releaseRanitidine Immediate release
68788-7423Ranitidine Immediate releaseRanitidine Immediate release
71610-359Ranitidine Immediate releaseRanitidine Immediate release
71610-371Ranitidine Immediate releaseRanitidine Immediate release
71610-378Ranitidine Immediate releaseRanitidine Immediate release
10202-8527 Select Acid ReducerRanitidine
0904-6350Acid ReducerRanitidine
0113-7950basic care acid reducerRanitidine
0113-7852basic care acid reducer 150Ranitidine
0113-7876basic care acid reducer 75Ranitidine
0113-0852Good Sense Acid ReducerRanitidine
0113-0876Good Sense Acid ReducerRanitidine
10202-712MAXIMUM STRENGTH RANITIDINERanitidine
0597-0121Maximum Strength Zantacranitidine
0121-0727RanitidineRANITIDINE
0121-4727RanitidineRANITIDINE
0172-4357RanitidineRanitidine
0172-4358RanitidineRanitidine
0363-0352RanitidineRanitidine
0440-8300RanitidineRanitidine
0440-8305RanitidineRanitidine
0615-4513RanitidineRanitidine
0615-4514RanitidineRanitidine
0615-8021RanitidineRanitidine
0781-6087RanitidineRanitidine
0904-6349RanitidineRanitidine
0904-6716RanitidineRanitidine
0904-6921RanitidineRanitidine
10544-056RanitidineRanitidine
10544-438RanitidineRanitidine
10544-516RanitidineRanitidine
11673-849RanitidineRanitidine
0904-6715ranitidine 75Ranitidine
11673-023up and up ranitidineRanitidine
0363-0852wal zan 150Ranitidine
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.