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"70771-1873-2" National Drug Code (NDC)
Tretinoin 1 TUBE in 1 CARTON (70771-1873-2) / 20 g in 1 TUBE
(Zydus Lifesciences Limited)
NDC Code
70771-1873-2
Package Description
1 TUBE in 1 CARTON (70771-1873-2) / 20 g in 1 TUBE
Product NDC
70771-1873
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Tretinoin
Non-Proprietary Name
Tretinoin
Dosage Form
CREAM
Usage
TOPICAL
Start Marketing Date
20240430
Marketing Category Name
ANDA
Application Number
ANDA218561
Manufacturer
Zydus Lifesciences Limited
Substance Name
TRETINOIN
Strength
1
Strength Unit
mg/g
Pharmacy Classes
Retinoid [EPC], Retinoids [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70771-1873-2