# Tilia Fe

NDC: 75907-086
Generic name: NdAc and EE Tablets and Ferrous Fumarate Tablets
Labeler / Manufacturer: Dr. Reddys Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: —
Marketing started: 20240601

FDA application: ANDA202962

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"75907-086"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=75907-086
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=118fb017-b44d-4223-ac5a-501ca96de210