Doxycycline Hyclate
- Product NDC
- 72143-211
- 11-digit product format
- 721430211
- Labeler code
- 72143
- Product ID
- 72143-211_74b2de40-77cd-4a58-b648-fbf036f48af0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- JG Pharma Inc.
- Application
- ANDA062269
- Marketing category
- ANDA
- Marketing start
- 2018-04-20
- Marketing end
- 2026-05-31
- Substance
- DOXYCYCLINE HYCLATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Current FDA listing
- Yes
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72143-211-60 | Doxycycline Hyclate | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72143-211 | DOXYCYCLINE HYCLATE TABLET, FILM COATED [JG PHARMA INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20200801_37a8cb92-0ade-4fbc-80f7-2ef283bc32cb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72143-211-60 | 72143021160 | 60 TABLET, FILM COATED in 1 BOTTLE (72143-211-60) | 2018-04-20 | 2026-05-31 | No | No | Current |