DOXYCYCLINE
- Product NDC
- 63629-6853
- 11-digit product format
- 636296853
- Labeler code
- 63629
- Product ID
- 63629-6853_cd4e0ac9-86a4-4af7-94b4-772fc85b2886
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXYCYCLINE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204234
- Marketing category
- ANDA
- Marketing start
- 2015-02-20
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6853-1 | 63629685301 | 20 CAPSULE in 1 BOTTLE (63629-6853-1) | 20 capsule | 2015-11-17 | 0000-00-00 | No | No | Current |
| 63629-6853-2 | 63629685302 | 28 CAPSULE in 1 BOTTLE (63629-6853-2) | 28 capsule | 2015-11-17 | 0000-00-00 | No | No | Current |
| 63629-6853-3 | 63629685303 | 30 CAPSULE in 1 BOTTLE (63629-6853-3) | 30 capsule | 2015-11-17 | 0000-00-00 | No | No | Current |