Doxycycline Hyclate
- Product NDC
- 63629-6880
- 11-digit product format
- 636296880
- Labeler code
- 63629
- Product ID
- 63629-6880_669b81b8-16e2-43e6-8916-d90658bc9cd2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA062677
- Marketing category
- ANDA
- Marketing start
- 1986-07-10
- 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 |
|---|
| 63629-6880-1 | 63629688001 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-6880-1) | 2016-01-14 | 0000-00-00 | No | No | Current |
| 63629-6880-2 | 63629688002 | 14 TABLET, FILM COATED in 1 BOTTLE (63629-6880-2) | 2016-01-14 | 0000-00-00 | No | No | Current |
| 63629-6880-3 | 63629688003 | 42 TABLET, FILM COATED in 1 BOTTLE (63629-6880-3) | 2016-01-14 | 0000-00-00 | No | No | Current |
| 63629-6880-4 | 63629688004 | 28 TABLET, FILM COATED in 1 BOTTLE (63629-6880-4) | 2016-01-14 | 0000-00-00 | No | No | Current |
| 63629-6880-5 | 63629688005 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-6880-5) | 2016-01-14 | 0000-00-00 | No | No | Current |