NDC 43063-844

Ranitidine

Ranitidine

Ranitidine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Pd-rx Pharmaceuticals, In. The primary component is Ranitidine Hydr.

Product ID43063-844_7cacc311-8de9-4c07-e053-2991aa0a38cd
NDC43063-844
Product TypeHuman Prescription Drug
Proprietary NameRanitidine
Generic NameRanitidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-12-16
Marketing CategoryANDA / ANDA
Application NumberANDA077824
Labeler NamePD-Rx Pharmaceuticals, In
Substance NameRANITIDINE HYDR
Active Ingredient Strength150 mg/1
Pharm ClassesHistamine H2 Re
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 43063-844-30

30 TABLET in 1 BOTTLE, PLASTIC (43063-844-30)
Marketing Start Date2018-04-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43063-844-60 [43063084460]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-04-11
Marketing End Date2019-09-18

NDC 43063-844-90 [43063084490]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-06-20
Marketing End Date2019-09-18

NDC 43063-844-30 [43063084430]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-04-06
Marketing End Date2019-09-18

NDC 43063-844-15 [43063084415]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-07-24
Marketing End Date2019-09-18

NDC 43063-844-20 [43063084420]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-07-03
Marketing End Date2019-09-18

NDC 43063-844-01 [43063084401]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-08-07
Marketing End Date2019-09-18

NDC 43063-844-14 [43063084414]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-05-17
Marketing End Date2019-09-18

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE150 mg/1

Pharmacological Class

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

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

NDCBrand NameGeneric Name
0121-0727RanitidineRANITIDINE
0121-4727RanitidineRANITIDINE
0172-4357RanitidineRanitidine
0172-4358RanitidineRanitidine
0363-0352RanitidineRanitidine
0440-2300RanitidineRanitidine Hydrochloride
0440-8300RanitidineRanitidine
0440-8305RanitidineRanitidine
0615-4513RanitidineRanitidine
0615-4514RanitidineRanitidine
0615-8021RanitidineRanitidine
0781-6087RanitidineRanitidine
0904-6349RanitidineRanitidine
0904-6716RanitidineRanitidine
0904-6921RanitidineRanitidine
10544-056RanitidineRanitidine
10544-438RanitidineRanitidine
10544-516RanitidineRanitidine
68071-2190RanitidineRanitidine
68071-3162RanitidineRanitidine
68071-3317RanitidineRanitidine
68071-2185RanitidineRanitidine
68071-3248RanitidineRanitidine
68071-3165RanitidineRanitidine
68151-1610RanitidineRanitidine
68151-2890RanitidineRanitidine
68462-248RanitidineRanitidine
68462-249RanitidineRanitidine
68788-6382RanitidineRanitidine
68788-7101RanitidineRanitidine
68788-7078RanitidineRanitidine
68788-7388RanitidineRanitidine
68788-9875RanitidineRanitidine
68788-9874RanitidineRanitidine
70408-141RANITIDINERANITIDINE
70518-0222RanitidineRanitidine
70518-0263RanitidineRanitidine
70518-0093RanitidineRanitidine
70518-0622RanitidineRanitidine
70518-0873RanitidineRanitidine
70518-0801RanitidineRanitidine
70518-1361RanitidineRanitidine
70518-1714RanitidineRanitidine
70934-017RanitidineRanitidine
71141-013RanitidineRanitidine
71335-0394RanitidineRanitidine
71335-0342RanitidineRanitidine
71335-0363RanitidineRanitidine
71821-001RanitidineRanitidine
71821-002RanitidineRanitidine

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