Doxycycline
- Product NDC
- 70518-0038
- 11-digit product format
- 705180038
- Labeler code
- 70518
- Product ID
- 70518-0038_e60fb8e0-b9a7-ca58-e053-2995a90afdcd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA091605
- Marketing category
- ANDA
- Marketing start
- 2016-12-05
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE
- Active strength
- 100 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 |
|---|
| 70518-0038-0 | 70518003800 | 40 TABLET in 1 BOTTLE (70518-0038-0) | 40 tablet | 2016-12-05 | 0000-00-00 | No | No | Current |
| 70518-0038-1 | 70518003801 | 14 TABLET in 1 BOTTLE, PLASTIC (70518-0038-1) | 14 tablet | 2022-07-13 | 0000-00-00 | No | No | Current |