NDC 10866-0271

NDC 10866-0271

NDC 10866-0271 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 10866-0271
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 10866-0271-1 [10866027101]

Stangard GEL
Marketing CategoryExport only
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1981-04-01

Drug Details


© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.