LINCOMYCIN
- Product NDC
- 52584-353
- 11-digit product format
- 525840353
- Labeler code
- 52584
- Product ID
- 52584-353_121cb853-ab09-459c-b5ea-ab2c8535a240
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lincomycin hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCONJUNCTIVAL
- Labeler
- General Injectables and Vaccines, INC.
- Application
- ANDA201746
- Marketing category
- ANDA
- Marketing start
- 2020-11-06
- Marketing end
- 2023-07-31
- Substance
- LINCOMYCIN HYDROCHLORIDE
- Active strength
- 300 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-353-05 | 52584035305 | 1 VIAL in 1 BAG (52584-353-05) > 10 mL in 1 VIAL | 1 vial | 2020-11-06 | 2023-07-31 | No | No | Current |