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"68387-310-30" National Drug Code (NDC)
Ranitidine Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-310-30)
(Keltman Pharmaceuticals Inc.)
NDC Code
68387-310-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68387-310-30)
Product NDC
68387-310
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine Hydrochloride
Non-Proprietary Name
Ranitidine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20090701
Marketing Category Name
ANDA
Application Number
ANDA074467
Manufacturer
Keltman Pharmaceuticals Inc.
Substance Name
RANITIDINE HYDROCHLORIDE
Strength
150
Strength Unit
mg/1
Pharmacy Classes
Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68387-310-30