Doxycycline Hyclate
- Product NDC
- 63629-8262
- 11-digit product format
- 636298262
- Labeler code
- 63629
- Product ID
- 63629-8262_740197b1-4c79-4d72-a36c-56a3f879925f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA062505
- Marketing category
- ANDA
- Marketing start
- 1984-09-11
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8262-1 | 63629826201 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-8262-1) | 2019-11-19 | 0000-00-00 | No | No | Current |
| 63629-8262-2 | 63629826202 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8262-2) | 2019-11-19 | 0000-00-00 | No | No | Current |
| 63629-8262-3 | 63629826203 | 50 TABLET, FILM COATED in 1 BOTTLE (63629-8262-3) | 2019-11-19 | 0000-00-00 | No | No | Current |