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"70771-1933-2" National Drug Code (NDC)
Tretinoin 1 TUBE in 1 CARTON (70771-1933-2) / 20 g in 1 TUBE
(Zydus Lifesciences Limited)
NDC Code
70771-1933-2
Package Description
1 TUBE in 1 CARTON (70771-1933-2) / 20 g in 1 TUBE
Product NDC
70771-1933
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Tretinoin
Non-Proprietary Name
Tretinoin
Dosage Form
CREAM
Usage
TOPICAL
Start Marketing Date
20261001
Marketing Category Name
ANDA
Application Number
ANDA218560
Manufacturer
Zydus Lifesciences Limited
Substance Name
TRETINOIN
Strength
.25
Strength Unit
mg/g
Pharmacy Classes
Retinoid [EPC], Retinoids [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70771-1933-2