Tetracycline Hydrochloride
- Product NDC
- 42291-799
- 11-digit product format
- 422910799
- Labeler code
- 42291
- Product ID
- 42291-799_d5c9d152-d260-153d-e053-2995a90a6a00
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tetracycline Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- AvKARE
- Application
- NDA050278
- Marketing category
- NDA
- Marketing start
- 2013-10-18
- Marketing end
- 0000-00-00
- Substance
- TETRACYCLINE HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Tetracycline-class Antimicrobial [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 42291-799-01 | 42291079901 | 100 CAPSULE in 1 BOTTLE (42291-799-01) | 100 capsule | 2017-08-08 | 0000-00-00 | No | No | Current |