Amoxicillin

Product NDC
71205-817
11-digit product format
712050817
Labeler code
71205
Product ID
71205-817_2c395111-c9c1-483e-a542-58b935ede689
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA065271
Marketing category
ANDA
Marketing start
2005-11-09
Substance
AMOXICILLIN
Active strength
500 mg/1
Pharmacologic classes
Penicillin-class Antibacterial [EPC], Penicillins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
804826J2HUAMOXICILLIN61336-70-7AMOXICILLIN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71205-817-147120508171414 CAPSULE in 1 BOTTLE (71205-817-14) 14 capsule2023-06-27NoNoHistorical
71205-817-207120508172020 CAPSULE in 1 BOTTLE (71205-817-20) 20 capsule2023-06-27NoNoHistorical
71205-817-217120508172121 CAPSULE in 1 BOTTLE (71205-817-21) 21 capsule2023-06-27NoNoHistorical
71205-817-307120508173030 CAPSULE in 1 BOTTLE (71205-817-30) 30 capsule2023-06-27NoNoHistorical
71205-817-407120508174040 CAPSULE in 1 BOTTLE (71205-817-40) 40 capsule2023-06-27NoNoHistorical
71205-817-607120508176060 CAPSULE in 1 BOTTLE (71205-817-60) 60 capsule2023-06-27NoNoHistorical
71205-817-907120508179090 CAPSULE in 1 BOTTLE (71205-817-90) 90 capsule2023-06-27NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AmoxicillinProficient Rx LP2023-08-01HUMAN PRESCRIPTION DRUG LABEL1