Doxycycline Hyclate
- Product NDC
- 60505-4382
- 11-digit product format
- 605054382
- Labeler code
- 60505
- Product ID
- 60505-4382_8f2020b8-f616-ceae-c7f2-099819460d76
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA209243
- Marketing category
- ANDA
- Marketing start
- 2019-08-01
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 75 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60505-4382 | DOXYCYCLINE HYCLATE TABLET, COATED [APOTEX CORP.] | 6 | Legacy NDC | 20250412_2aa7ec9a-94b7-2f89-0d52-af9ec610b8fa.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-4382-6 | 60505438206 | 60 TABLET, COATED in 1 BOTTLE (60505-4382-6) | 2019-08-01 | 0000-00-00 | No | No | Current |