Proparacaine Hydrochloride

Product NDC
68071-1332
11-digit product format
680711332
Labeler code
68071
Product ID
68071-1332_589aba9d-52b3-1197-e053-2a91aa0aab41
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Proparacaine Hydrochloride
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA040074
Marketing category
ANDA
Marketing start
1995-09-29
Marketing end
0000-00-00
Substance
PROPARACAINE HYDROCHLORIDE
Active strength
5 mg/mL
Pharmacologic classes
Local Anesthesia [PE],Local Anesthetic [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-1332-52021-04-16C16284748780-1ba0f9c33-2cb5-a910-e053-dadaa90a0b85589ac17c-9400-e481-e053-2991aa0adbb5
68071-1332-52021-01-29C16284748780-1ba0f9c33-2cb5-a910-e053-dadaa90a0b85589ac17c-9400-e481-e053-2991aa0adbb5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68071-1332-5ML - Milliliter68071-1332753c0df9-95da-41a5-b0f3-6d2f458cd4d712017-09-11