LymePak
- Product NDC
- 72336-596
- 11-digit product format
- 723360596
- Labeler code
- 72336
- Product ID
- 72336-596_cb7504ac-ff58-1d9e-e053-2995a90a1d46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline Hyclate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- LIFSA DRUGS LLC
- Application
- NDA209844
- Marketing category
- NDA
- Marketing start
- 2021-09-10
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72336-596-87 | 72336059687 | 3 BLISTER PACK in 1 CARTON (72336-596-87) > 14 TABLET, FILM COATED in 1 BLISTER PACK (72336-596-86) | 3 blister pack | 2021-09-10 | 0000-00-00 | No | No | Current |