Lincocin
- Product NDC
- 0009-0555
- 11-digit product format
- 000090555
- Labeler code
- 0009
- Product ID
- 0009-0555_85e116ab-c3c1-47d1-8924-825d3e588c2d
- 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
- 1964-12-29
- Marketing end
- 0000-00-00
- Substance
- LINCOMYCIN HYDROCHLORIDE
- Active strength
- 300 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0009-0555-01 | Lincocin | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | | 29 |
| 0009-0555-01 | Lincocin | 2 mL in 1 VIAL | INJECTION, SOLUTION | 2 | | 29 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0009-0555 | LINCOCIN (LINCOMYCIN HYDROCHLORIDE) INJECTION, SOLUTION [PHARMACIA & UPJOHN COMPANY LLC] | 29 | Legacy NDC, 2 package rows | 20250313_c01906fa-2c73-4c13-9765-2fd06628d263.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0009-0555-01 | 00009055501 | 1 VIAL in 1 CARTON (0009-0555-01) > 2 mL in 1 VIAL | 1 vial | 1964-12-29 | 0000-00-00 | No | No | Current |
| 0009-0555-02 | 00009055502 | 10 mL in 1 VIAL (0009-0555-02) | 10 ml | 1964-12-29 | 0000-00-00 | No | No | Current |