DOXYCYCLINE
- Product NDC
- 52584-437
- 11-digit product format
- 525840437
- Labeler code
- 52584
- Product ID
- 52584-437_7cf5223a-9575-4e62-9058-cb72cdb62b75
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxycycline
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- ANDA091406
- Marketing category
- ANDA
- Marketing start
- 2019-12-20
- Marketing end
- 2023-02-28
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 100 mg/10mL
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- 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 |
|---|
| 52584-437-00 | 52584043700 | 1 PACKAGE in 1 BAG (52584-437-00) > 10 mL in 1 PACKAGE | 1 package | 2019-12-20 | 0000-00-00 | No | No | Current |