oxybutynin chloride
- Product NDC
- 71335-0610
- 11-digit product format
- 713350610
- Labeler code
- 71335
- Product ID
- 71335-0610_96a9d017-326b-4fd0-8036-c7660d3f469e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxybutynin chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207138
- Marketing category
- ANDA
- Marketing start
- 2016-12-20
- Marketing end
- 0000-00-00
- Substance
- OXYBUTYNIN CHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0610-1 | 71335061001 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0610-1) | 2017-12-01 | 0000-00-00 | No | No | Current |
| 71335-0610-2 | 71335061002 | 18 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0610-2) | 2017-12-01 | 0000-00-00 | No | No | Current |
| 71335-0610-3 | 71335061003 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0610-3) | 2017-12-01 | 0000-00-00 | No | No | Current |
| 71335-0610-4 | 71335061004 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0610-4) | 2017-12-01 | 0000-00-00 | No | No | Current |