United States · FDA National Drug Code directory
Lincomycin
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
- 0121-1035_23f95ea6-ad32-a143-e063-6394a90ae77c
- Product NDC
- 0121-1035
- Form
- INJECTION
- Composition / generic term
- Lincomycin Hydrochloride
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241007
- Source listing expiry
- 20261231
Source-listed ingredients
- LINCOMYCIN HYDROCHLORIDE — 3000 mg/10mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, MULTI-DOSE in 1 CARTON (0121-1035-55) / 10 mL in 1 VIAL, MULTI-DOSE · 0121-1035-55
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →