United States · FDA National Drug Code directory

Tilia Fe

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 75907-086_af37ed43-957f-4f93-935c-6c2158ab0e15
Product NDC: 75907-086
Form: KIT
Composition / generic term: NdAc and EE Tablets and Ferrous Fumarate Tablets
Labeler: Dr. Reddys Laboratories Inc.
Marketing category: ANDA
Marketing start / end (source format): 20240601
Source listing expiry: 20261231

Source-listed ingredients

Separate ingredient quantities are not available in this snapshot. Any composition term above is preserved as source text.

These values do not establish equivalence or a dose recommendation.

Packages

1 BLISTER PACK in 1 PACKET (75907-086-28) / 1 KIT in 1 BLISTER PACK · 75907-086-28
3 BLISTER PACK in 1 CARTON (75907-086-32) / 1 KIT in 1 BLISTER PACK · 75907-086-32

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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