Doxycycline
- Product NDC
- 70934-808
- 11-digit product format
- 709340808
- Labeler code
- 70934
- Product ID
- 70934-808_b6bf34ef-7e12-f214-e053-2a95a90a2ba3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA065285
- Marketing category
- ANDA
- Marketing start
- 2020-12-04
- 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
- 2021-12-31
- 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 |
|---|
| 70934-808-20 | 70934080820 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-808-20) | 2020-12-04 | 0000-00-00 | No | No | Current |