Lincocin
- Product NDC
- 0009-0107
- 11-digit product format
- 000090107
- Labeler code
- 0009
- Product ID
- 0009-0107_7e2f3780-88ee-4971-a4ab-3d6cd972c42c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lincomycin hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCONJUNCTIVAL
- Labeler
- Pharmacia & Upjohn Company LLC
- Application
- NDA050317
- Marketing category
- NDA
- Marketing start
- 2023-04-18
- Substance
- LINCOMYCIN HYDROCHLORIDE
- Active strength
- 300 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| M6T05Z2B68 | LINCOMYCIN HYDROCHLORIDE | 7179-49-9 | LINCOMYCIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0009-0107-04 | 00009010704 | 1 VIAL in 1 CARTON (0009-0107-04) / 10 mL in 1 VIAL | 1 vial | 2023-04-18 | No | No | Historical |