Tetracycline Hydrochloride
- Product NDC
- 47781-509
- 11-digit product format
- 477810509
- Labeler code
- 47781
- Product ID
- 47781-509_bd44a758-a900-098e-1090-db489b7aa32d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tetracycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Alvogen Inc.
- Application
- ANDA062752
- Marketing category
- ANDA
- Marketing start
- 2016-12-19
- Marketing end
- 2022-04-01
- Substance
- TETRACYCLINE HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Tetracycline-class Antimicrobial [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 |
|---|
| 47781-509-01 | 47781050901 | 100 CAPSULE in 1 BOTTLE (47781-509-01) | 100 capsule | 2016-12-19 | 2022-04-01 | No | No | Current |