Doxycycline Hyclate
- Product NDC
- 70518-3135
- 11-digit product format
- 705183135
- Labeler code
- 70518
- Product ID
- 70518-3135_f213753d-7d4e-25f1-e053-2995a90a1b27
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA062505
- Marketing category
- ANDA
- Marketing start
- 2021-06-25
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3135-0 | 70518313500 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3135-0) | 2021-06-25 | 0000-00-00 | No | No | Current |
| 70518-3135-1 | 70518313501 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3135-1) | 2023-01-09 | 0000-00-00 | No | No | Current |