Ranitidine

Product NDC
43063-087
11-digit product format
430630087
Labeler code
43063
Product ID
43063-087_8b3af210-309a-8c10-e053-2a95a90a86f1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ranitidine
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA077824
Marketing category
ANDA
Marketing start
2009-12-16
Marketing end
0000-00-00
Substance
RANITIDINE HYDROCHLORIDE
Active strength
300 mg/1
Pharmacologic classes
Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
43063-087-14EA - Each43063-08748574ed9-795a-47e8-9485-26ed2b5698eb12018-06-11
43063-087-30EA - Each43063-087ca17a5a3-4afd-408b-94e6-6d8cd0b38dd512018-06-11
43063-087-60EA - Each43063-087a0cc00b3-d7c5-4dc0-b746-55d0f5b7515812013-05-02