Demeclocycline Hydrochloride

Product NDC
42291-264
11-digit product format
422910264
Labeler code
42291
Product ID
42291-264_636137da-63e6-1e0b-e053-2991aa0a5d3e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Demeclocycline
Dosage form
TABLET
Route
ORAL
Labeler
AvKARE, Inc.
Application
ANDA065425
Marketing category
ANDA
Marketing start
2017-04-27
Marketing end
0000-00-00
Substance
DEMECLOCYCLINE HYDROCHLORIDE
Active strength
150 mg/1
Pharmacologic classes
Tetracycline-class Antimicrobial [EPC],Tetracyclines [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42291-264-01EA - Each42291-2646fd41161-e3c8-45c1-b21f-1c339822f63912017-06-15