DOXYCYCLINE
- Product NDC
- 70518-3365
- 11-digit product format
- 705183365
- Labeler code
- 70518
- Product ID
- 70518-3365_e83dfff2-dded-562a-e053-2995a90aa7a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXYCYCLINE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204234
- Marketing category
- ANDA
- Marketing start
- 2022-02-14
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [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 |
|---|
| 70518-3365-0 | 70518336500 | 60 CAPSULE in 1 BOTTLE, PLASTIC (70518-3365-0) | 60 capsule | 2022-02-14 | 0000-00-00 | No | No | Current |