United States · FDA National Drug Code directory
allergy relief
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
- 0363-1612_eff828bf-472b-4f68-a285-a7952c1d4a56
- Product NDC
- 0363-1612
- Form
- TABLET
- Composition / generic term
- Loratadine
- Labeler
- Walgreen Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211021
- Source listing expiry
- 20271231
Source-listed ingredients
- LORATADINE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (0363-1612-03) / 70 TABLET in 1 BOTTLE · 0363-1612-03
- 1 BOTTLE in 1 CARTON (0363-1612-47) / 150 TABLET in 1 BOTTLE · 0363-1612-47
- 1 BOTTLE in 1 CARTON (0363-1612-58) / 40 TABLET in 1 BOTTLE · 0363-1612-58
- 1 BOTTLE in 1 CARTON (0363-1612-65) / 30 TABLET in 1 BOTTLE · 0363-1612-65
- 1 BOTTLE in 1 CARTON (0363-1612-78) / 100 TABLET in 1 BOTTLE · 0363-1612-78
- 1 BOTTLE in 1 CARTON (0363-1612-88) / 365 TABLET in 1 BOTTLE · 0363-1612-88
- 1 BOTTLE in 1 CARTON (0363-1612-95) / 45 TABLET in 1 BOTTLE · 0363-1612-95
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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