Doxycycline Hyclate
- Product NDC
- 70934-187
- 11-digit product format
- 709340187
- Labeler code
- 70934
- Product ID
- 70934-187_a500521b-fe2f-7759-e053-2995a90a9885
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA062269
- Marketing category
- ANDA
- Marketing start
- 2020-02-24
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-187-20 | 70934018720 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-187-20) | 2020-03-25 | 0000-00-00 | No | No | Current |
| 70934-187-30 | 70934018730 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-187-30) | 2020-02-24 | 0000-00-00 | No | No | Current |